A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3526579



Internal ID18478174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:57862421..58101731hg38UCSC Ensembl
Innerchr13:58436555..58675865hg19UCSC Ensembl
Innerchr13:57334556..57573866hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg38239311
hg19239311
hg18239311
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036017
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)nssv3526579
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer