A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3714928



Internal ID19013209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18592436..18844391hg38UCSC Ensembl
Innerchr13:19166576..19418531hg19UCSC Ensembl
Innerchr13:18064576..18316531hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg38251956
hg19251956
hg18251956
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044688
Supporting Variants
Samples
Known GenesANKRD20A9P, LINC00417
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3714928
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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