A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700218



Internal ID15436870
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524316
Supporting Variants
Samples
Known GenesCDK14
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700218
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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