A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998106



Internal ID18810956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:138132356..138215768hg38UCSC Ensembl
Innerchr3:137851198..137934610hg19UCSC Ensembl
Innerchr3:139333888..139417300hg18UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3883413
hg1983413
hg1883413
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3741472
Samples
Known GenesA4GNT, ARMC8, DBR1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998106
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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