A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv654177



Internal ID15044143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:63877111..63906241hg38UCSC Ensembl
Innerchr17:61954471..61983601hg19UCSC Ensembl
Innerchr17:59308203..59337333hg18UCSC Ensembl
Innerchr17:59308203..59337333hg17UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg3829131
hg1929131
hg1829131
hg1729131
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517272
Supporting Variants
Samples
Known GenesCSH1, GH2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv654177
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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