A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894034



Internal ID18838202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:111801745..111814479hg38UCSC Ensembl
Outerchr1:111801745..111814479hg38UCSC Ensembl
Innerchr1:112344367..112357101hg19UCSC Ensembl
Outerchr1:112344367..112357101hg19UCSC Ensembl
Innerchr1:112145890..112158624hg18UCSC Ensembl
Outerchr1:112145890..112158624hg18UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg3812735
hg1912735
hg1812735
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780886
Samples
Known GenesKCND3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894034
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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