A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25781279



Internal ID19175002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:119873770..119941158hg38UCSC Ensembl
Innerchr6:120194916..120262304hg19UCSC Ensembl
Innerchr6:120236615..120304003hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3867389
hg1967389
hg1867389
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890932
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=17
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25781279
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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