A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038169



Internal ID18780700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:24694944..24752415hg38UCSC Ensembl
Innerchr13:25269082..25326553hg19UCSC Ensembl
Innerchr13:24167082..24224553hg18UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg3857472
hg1957472
hg1857472
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1621n100
Supporting Variantsnssv3714954
Samples
Known GenesATP12A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038169
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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