A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25781464



Internal ID19168204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:196854170..196886173hg38UCSC Ensembl
Innerchr1:196823300..196855303hg19UCSC Ensembl
Innerchr1:195089923..195121926hg18UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg3832004
hg1932004
hg1832004
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891015
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=9
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25781464
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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