A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891626



Internal ID19186022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17039314..17071164hg38UCSC Ensembl
Outerchr9:17039314..17071164hg38UCSC Ensembl
Innerchr9:17039312..17071162hg19UCSC Ensembl
Outerchr9:17039312..17071162hg19UCSC Ensembl
Innerchr9:17029312..17061162hg18UCSC Ensembl
Outerchr9:17029312..17061162hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3831851
hg1931851
hg1831851
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781674
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891626
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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