A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv658145



Internal ID15394797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:94343049..94496272hg38UCSC Ensembl
Innerchr12:94736825..94890048hg19UCSC Ensembl
Innerchr12:93260956..93414179hg18UCSC Ensembl
Innerchr12:93239293..93392516hg17UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38153224
hg19153224
hg18153224
hg17153224
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516550
Supporting Variants
Samples
Known GenesCCDC41, CCDC41-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv658145
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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