A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6395628



Internal ID9768159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:195465202..195466678hg38UCSC Ensembl
Outerchr3:195465165..195466728hg38UCSC Ensembl
Innerchr3:195185920..195187397hg19UCSC Ensembl
Outerchr3:195185883..195187447hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg381564
hg191565
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2667844
Supporting Variants
SamplesNA19725
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6395628
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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