A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3526580



Internal ID18478175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:58190235..58462870hg38UCSC Ensembl
Innerchr13:58764369..59037004hg19UCSC Ensembl
Innerchr13:57662370..57935005hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg38272636
hg19272636
hg18272636
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049570
Supporting Variants
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)nssv3526580
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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