A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv678184



Internal ID15414836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:37491309..37544959hg38UCSC Ensembl
Innerchr13:38065446..38119096hg19UCSC Ensembl
Innerchr13:36963446..37017096hg18UCSC Ensembl
Innerchr13:36963446..37017096hg17UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3853651
hg1953651
hg1853651
hg1753651
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517476
Supporting Variants
Samples
Known GenesLINC00547
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv678184
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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