A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615245



Internal ID7002134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140968819..140973458hg38UCSC Ensembl
Innerchr7:140968819..140973458hg38UCSC Ensembl
Outerchr7:140968782..140973529hg38UCSC Ensembl
chr7:140668619..140673258hg19UCSC Ensembl
Innerchr7:140668619..140673258hg19UCSC Ensembl
Outerchr7:140668582..140673329hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg384640
hg194640
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12985095
SamplesHG03135
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615245
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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