A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv670434



Internal ID15407086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:116336585..116373151hg38UCSC Ensembl
Innerchr11:116207302..116243868hg19UCSC Ensembl
Innerchr11:115712512..115749078hg18UCSC Ensembl
Innerchr11:115712512..115749078hg17UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3836567
hg1936567
hg1836567
hg1736567
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516720
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv670434
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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