A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524234



Internal ID15104841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:45505316..45580555hg38UCSC Ensembl
Innerchr17:43582682..43657921hg19UCSC Ensembl
Innerchr17:40938465..41013704hg18UCSC Ensembl
Innerchr17:40938465..41013704hg17UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3875240
hg1975240
hg1875240
hg1775240
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700124
Samples
Known GenesLRRC37A4P
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524234
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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