A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25786564



Internal ID18823507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:39160735..39170912hg38UCSC Ensembl
Innerchr17:37316988..37327165hg19UCSC Ensembl
Innerchr17:34570514..34580691hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3810178
hg1910178
hg1810178
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893011
Supporting Variants
Samples
Known GenesARL5C
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=8
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25786564
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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