A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037959



Internal ID19127178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:26802474..26837122hg38UCSC Ensembl
Innerchr13:27376611..27411259hg19UCSC Ensembl
Innerchr13:26274611..26309259hg18UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3834649
hg1934649
hg1834649
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1623n100
Supporting Variantsnssv3523212
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)nsv1037959
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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