A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3523465



Internal ID18821746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:51970669..52007365hg38UCSC Ensembl
Innerchr13:52544805..52581501hg19UCSC Ensembl
Innerchr13:51442806..51479502hg18UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg3836697
hg1936697
hg1836697
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041996
Supporting Variants
Samples
Known GenesATP7B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3523465
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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