A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv673775



Internal ID15410427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:127843238..127845323hg38UCSC Ensembl
Innerchr10:129641502..129643587hg19UCSC Ensembl
Innerchr10:129531492..129533577hg18UCSC Ensembl
Innerchr10:129531492..129533577hg17UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg382086
hg192086
hg182086
hg172086
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520082
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv673775
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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