A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892138



Internal ID18839848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:10430766..10530730hg38UCSC Ensembl
Outerchr12:10430766..10530730hg38UCSC Ensembl
Innerchr12:10583365..10683329hg19UCSC Ensembl
Outerchr12:10583365..10683329hg19UCSC Ensembl
Innerchr12:10474632..10574596hg18UCSC Ensembl
Outerchr12:10474632..10574596hg18UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3899965
hg1999965
hg1899965
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784841
Samples
Known GenesKLRC1, KLRC2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892138
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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