A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704637



Internal ID15441289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:128628713..128634536hg38UCSC Ensembl
Innerchr10:130426977..130432800hg19UCSC Ensembl
Innerchr10:130316967..130322790hg18UCSC Ensembl
Innerchr10:130316967..130322790hg17UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg385824
hg195824
hg185824
hg175824
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528097
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704637
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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