A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv663796



Internal ID15053762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:91272737..91283251hg38UCSC Ensembl
Innerchr14:91739081..91749595hg19UCSC Ensembl
Innerchr14:90808834..90819348hg18UCSC Ensembl
Innerchr14:90808834..90819348hg17UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg3810515
hg1910515
hg1810515
hg1710515
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517700
Supporting Variants
Samples
Known GenesCCDC88C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv663796
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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