A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890877



Internal ID19185179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:71186742..71223569hg38UCSC Ensembl
Outerchr6:71186742..71223569hg38UCSC Ensembl
Innerchr6:71896445..71933272hg19UCSC Ensembl
Outerchr6:71896445..71933272hg19UCSC Ensembl
Innerchr6:71953166..71989993hg18UCSC Ensembl
Outerchr6:71953166..71989993hg18UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3836828
hg1936828
hg1836828
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779456
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890877
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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