A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010762



Internal ID19099979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:101865992..102084977hg38UCSC Ensembl
Innerchr3:101584836..101803821hg19UCSC Ensembl
Innerchr3:103067526..103286511hg18UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg38218986
hg19218986
hg18218986
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3604372
Samples
Known GenesLOC152225
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010762
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer