A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524316



Internal ID15451609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:91165480..91171472hg38UCSC Ensembl
Innerchr7:90794795..90800787hg19UCSC Ensembl
Innerchr7:90632731..90638723hg18UCSC Ensembl
Innerchr7:90439446..90445438hg17UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg385993
hg195993
hg185993
hg175993
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700218
Samples
Known GenesCDK14
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524316
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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