A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3523326



Internal ID18821607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:37502522..37540973hg38UCSC Ensembl
Innerchr13:38076659..38115110hg19UCSC Ensembl
Innerchr13:36974659..37013110hg18UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3838452
hg1938452
hg1838452
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042563
Supporting Variants
Samples
Known GenesLINC00547
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3523326
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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