A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3525529



Internal ID18477124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:100521000..100622872hg38UCSC Ensembl
Innerchr13:101173254..101275126hg19UCSC Ensembl
Innerchr13:99971255..100073127hg18UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38101873
hg19101873
hg18101873
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037414
Supporting Variants
Samples
Known GenesGGACT, PCCA, TMTC4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3525529
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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