A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702153



Internal ID15092119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:3072453..3077561hg38UCSC Ensembl
Innerchr10:3114645..3119753hg19UCSC Ensembl
Innerchr10:3104645..3109753hg18UCSC Ensembl
Innerchr10:3104645..3109753hg17UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg385109
hg195109
hg185109
hg175109
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517630
Supporting Variants
Samples
Known GenesPFKP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702153
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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