A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv685789



Internal ID15075755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:117968137..118028672hg38UCSC Ensembl
Innerchr10:119727648..119788183hg19UCSC Ensembl
Innerchr10:119717638..119778173hg18UCSC Ensembl
Innerchr10:119717638..119778173hg17UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg3860536
hg1960536
hg1860536
hg1760536
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516870
Supporting Variants
Samples
Known GenesRAB11FIP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv685789
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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