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dbVar

Database of genomic structural variation

nsv4420905

Organism: Homo sapiens

Study:nstd174 (DGV Gold Standard)
Variant Type:copy number variation
Method Type:Multiple
Submitted on:GRCh37 (hg19)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:79,177

Links to Other Resources

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 278 SVs from 49 studies. See in: genome view

Remapped(Score: Perfect):103,385,173-103,464,349

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nsv4420905	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000010.11	Chr10	103,385,173	103,396,772	103,460,344	103,464,349
nsv4420905	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000010.10	Chr10	105,144,930	105,156,529	105,220,101	105,224,106

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv15708488	copy number gain	Multiple	Multiple

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nssv15708488	Remapped	Perfect	NC_000010.11:g.(10 3385173_103396772) _(103460344_103464 349)dup	GRCh38.p12	First Pass	NC_000010.11	Chr10	103,385,173	103,396,772	103,460,344	103,464,349
nssv15708488	Submitted genomic		NC_000010.10:g.(10 5144930_105156529) _(105220101_105224 106)dup	GRCh37 (hg19)		NC_000010.10	Chr10	105,144,930	105,156,529	105,220,101	105,224,106

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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