A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891232



Internal ID19185628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:148628234..148660487hg38UCSC Ensembl
Outerchr7:148628234..148660487hg38UCSC Ensembl
Innerchr7:148325326..148357579hg19UCSC Ensembl
Outerchr7:148325326..148357579hg19UCSC Ensembl
Innerchr7:147956259..147988512hg18UCSC Ensembl
Outerchr7:147956259..147988512hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3832254
hg1932254
hg1832254
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797954
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891232
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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