A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516725



Internal ID15444018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:68856443..68859103hg38UCSC Ensembl
Innerchr10:70616199..70618859hg19UCSC Ensembl
Innerchr10:70286205..70288865hg18UCSC Ensembl
Innerchr10:70286205..70288865hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg382661
hg192661
hg182661
hg172661
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv683773, nssv685721, nssv670464, nssv680464
Samples
Known GenesSTOX1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516725
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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