A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997756



Internal ID18810606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:111507211..111657738hg38UCSC Ensembl
Innerchr3:111226058..111376585hg19UCSC Ensembl
Innerchr3:112708748..112859275hg18UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg38150528
hg19150528
hg18150528
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3604414
Samples
Known GenesCD96, ZBED2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997756
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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