A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614018



Internal ID7000913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:86666303..86676756hg38UCSC Ensembl
Innerchr7:86666316..86676744hg38UCSC Ensembl
Outerchr7:86666291..86676769hg38UCSC Ensembl
chr7:86295619..86306072hg19UCSC Ensembl
Innerchr7:86295632..86306060hg19UCSC Ensembl
Outerchr7:86295607..86306085hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3810454
hg1910454
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12878777
SamplesHG01961
Known GenesGRM3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614018
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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