A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5647931



Internal ID9127826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:113044918..113047210hg38UCSC Ensembl
Outerchr3:113044884..113047245hg38UCSC Ensembl
Innerchr3:112763765..112766057hg19UCSC Ensembl
Outerchr3:112763731..112766092hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg382362
hg192362
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658713
Supporting Variants
SamplesHG01149
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5647931
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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