A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv663438



Internal ID15053404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:3108122..3113598hg38UCSC Ensembl
Innerchr10:3150314..3155790hg19UCSC Ensembl
Innerchr10:3140314..3145790hg18UCSC Ensembl
Innerchr10:3140314..3145790hg17UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg385477
hg195477
hg185477
hg175477
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516811
Supporting Variants
Samples
Known GenesPFKP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv663438
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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