A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663173



Internal ID9929278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:24430223..24433114hg38UCSC Ensembl
Outerchr7:24430186..24433164hg38UCSC Ensembl
Innerchr7:24469842..24472733hg19UCSC Ensembl
Outerchr7:24469805..24472783hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg382979
hg192979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5546765
SamplesHG00583
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663173
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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