A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893033



Internal ID18837167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:60245368..60377776hg38UCSC Ensembl
Outerchr17:60245368..60377776hg38UCSC Ensembl
Innerchr17:58322729..58455137hg19UCSC Ensembl
Outerchr17:58322729..58455137hg19UCSC Ensembl
Innerchr17:55677511..55809919hg18UCSC Ensembl
Outerchr17:55677511..55809919hg18UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38132409
hg19132409
hg18132409
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784821
Samples
Known GenesUSP32
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893033
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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