A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv673199



Internal ID15063165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86680650..86680809hg38UCSC Ensembl
Innerchr10:88440407..88440566hg19UCSC Ensembl
Innerchr10:88430387..88430546hg18UCSC Ensembl
Innerchr10:88430387..88430546hg17UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38160
hg19160
hg18160
hg17160
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517139
Supporting Variants
Samples
Known GenesLDB3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv673199
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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