A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998309



Internal ID18811159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:112411443..112559957hg38UCSC Ensembl
Innerchr3:112130290..112278804hg19UCSC Ensembl
Innerchr3:113612980..113761494hg18UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg38148515
hg19148515
hg18148515
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4840n100
Supporting Variantsnssv3604445
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)nsv998309
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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