A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890932



Internal ID19185328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:119873770..119941158hg38UCSC Ensembl
Outerchr6:119873770..119941158hg38UCSC Ensembl
Innerchr6:120194916..120262304hg19UCSC Ensembl
Outerchr6:120194916..120262304hg19UCSC Ensembl
Innerchr6:120236615..120304003hg18UCSC Ensembl
Outerchr6:120236615..120304003hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3867389
hg1967389
hg1867389
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781279
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890932
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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