A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613700



Internal ID7000596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74159245..74161413hg38UCSC Ensembl
Innerchr7:74159279..74161380hg38UCSC Ensembl
Outerchr7:74159212..74161447hg38UCSC Ensembl
chr7:73573575..73575743hg19UCSC Ensembl
Innerchr7:73573609..73575710hg19UCSC Ensembl
Outerchr7:73573542..73575777hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg382169
hg192169
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12843181
SamplesNA19455
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613700
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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