A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668696



Internal ID15058662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:13015323..13018410hg38UCSC Ensembl
Innerchr10:13057323..13060410hg19UCSC Ensembl
Innerchr10:13097329..13100416hg18UCSC Ensembl
Innerchr10:13097329..13100416hg17UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg383088
hg193088
hg183088
hg173088
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516198
Supporting Variants
Samples
Known GenesCCDC3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668696
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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