A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv685752



Internal ID15075718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:89180930..89186051hg38UCSC Ensembl
Innerchr10:90940687..90945808hg19UCSC Ensembl
Innerchr10:90930667..90935788hg18UCSC Ensembl
Innerchr10:90930667..90935788hg17UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg385122
hg195122
hg185122
hg175122
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517170
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv685752
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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