A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613632



Internal ID6653841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:71581607..71582718hg38UCSC Ensembl
Innerchr7:71581652..71582673hg38UCSC Ensembl
Outerchr7:71581562..71582763hg38UCSC Ensembl
chr7:71046592..71047703hg19UCSC Ensembl
Innerchr7:71046637..71047658hg19UCSC Ensembl
Outerchr7:71046547..71047748hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg381112
hg191112
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12829713
SamplesHG02787
Known GenesWBSCR17
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613632
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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