A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890903



Internal ID19185299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:89552180..89637792hg38UCSC Ensembl
Outerchr6:89552180..89637792hg38UCSC Ensembl
Innerchr6:90261899..90347511hg19UCSC Ensembl
Outerchr6:90261899..90347511hg19UCSC Ensembl
Innerchr6:90318618..90404232hg18UCSC Ensembl
Outerchr6:90318618..90404232hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3885613
hg1985613
hg1885615
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792687
Samples
Known GenesANKRD6, LYRM2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890903
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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