A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv690234



Internal ID15426886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:3123124..3124432hg38UCSC Ensembl
Innerchr10:3165316..3166624hg19UCSC Ensembl
Innerchr10:3155316..3156624hg18UCSC Ensembl
Innerchr10:3155316..3156624hg17UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg381309
hg191309
hg181309
hg171309
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516917
Supporting Variants
Samples
Known GenesPFKP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv690234
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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