A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3711831



Internal ID19010112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:63849994..64388006hg38UCSC Ensembl
Innerchr13:64424127..64962138hg19UCSC Ensembl
Innerchr13:63322128..63860139hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38538013
hg19538012
hg18538012
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047229
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)nssv3711831
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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