A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3526585



Internal ID18824866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:60181103..60226799hg38UCSC Ensembl
Innerchr13:60755237..60800933hg19UCSC Ensembl
Innerchr13:59653238..59698934hg18UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg3845697
hg1945697
hg1845697
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040294
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)nssv3526585
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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