A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3526568



Internal ID18824849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:57361787..57404521hg38UCSC Ensembl
Innerchr13:57935921..57978655hg19UCSC Ensembl
Innerchr13:56833922..56876656hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3842735
hg1942735
hg1842735
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1038125
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)nssv3526568
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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