A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695303



Internal ID15085269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:3113348..3113506hg38UCSC Ensembl
Innerchr10:3155540..3155698hg19UCSC Ensembl
Innerchr10:3145540..3145698hg18UCSC Ensembl
Innerchr10:3145540..3145698hg17UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg38159
hg19159
hg18159
hg17159
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)nssv695303
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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