A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703992



Internal ID15440644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:89608881..89611264hg38UCSC Ensembl
Innerchr10:91368638..91371021hg19UCSC Ensembl
Innerchr10:91358618..91361001hg18UCSC Ensembl
Innerchr10:91358618..91361001hg17UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg382384
hg192384
hg182384
hg172384
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527532
Supporting Variants
Samples
Known GenesPANK1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703992
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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