A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010619



Internal ID18753151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:100634965..100670413hg38UCSC Ensembl
Innerchr3:100353809..100389257hg19UCSC Ensembl
Innerchr3:101836499..101871947hg18UCSC Ensembl
Cytoband3q12.2
Allele length
AssemblyAllele length
hg3835449
hg1935449
hg1835449
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3604367
Samples
Known GenesGPR128
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010619
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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