A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25781109



Internal ID19167164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:33640660..33652165hg38UCSC Ensembl
Innerchr17:31967679..31979184hg19UCSC Ensembl
Innerchr17:28991792..29003297hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3811506
hg1911506
hg1811506
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892995
Supporting Variants
Samples
Known GenesASIC2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=9
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25781109
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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