A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3711765



Internal ID18663360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:58191397..58251260hg38UCSC Ensembl
Innerchr13:58765531..58825394hg19UCSC Ensembl
Innerchr13:57663532..57723395hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3859864
hg1959864
hg1859864
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035909
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)nssv3711765
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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