A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780886



Internal ID18819883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:111801745..111814479hg38UCSC Ensembl
Innerchr1:112344367..112357101hg19UCSC Ensembl
Innerchr1:112145890..112158624hg18UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg3812735
hg1912735
hg1812735
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3894034
Supporting Variants
Samples
Known GenesKCND3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=11
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780886
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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