A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003936



Internal ID18746467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:112407084..112555766hg38UCSC Ensembl
Innerchr3:112125931..112274613hg19UCSC Ensembl
Innerchr3:113608621..113757303hg18UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg38148683
hg19148683
hg18148683
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4840n100
Supporting Variantsnssv3604444
Samples
Known GenesATG3, BTLA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1003936
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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