A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5478626



Internal ID9521396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:57968370..57991985hg38UCSC Ensembl
Outerchr3:57968207..57992138hg38UCSC Ensembl
Innerchr3:57954097..57977712hg19UCSC Ensembl
Outerchr3:57953934..57977865hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg3823932
hg1923932
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2665213
Supporting Variants
SamplesNA19009
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5478626
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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