A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022031



Internal ID19111249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:64043327..64156650hg38UCSC Ensembl
Innerchr5:63339154..63452477hg19UCSC Ensembl
Innerchr5:63374910..63488233hg18UCSC Ensembl
Cytoband5q12.2
Allele length
AssemblyAllele length
hg38113324
hg19113324
hg18113324
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3640787
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022031
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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