A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614982



Internal ID7001871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:128605973..128663472hg38UCSC Ensembl
Innerchr7:128605973..128663472hg38UCSC Ensembl
Outerchr7:128605473..128663972hg38UCSC Ensembl
chr7:128246027..128303526hg19UCSC Ensembl
Innerchr7:128246027..128303526hg19UCSC Ensembl
Outerchr7:128245527..128304026hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg3857500
hg1957500
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12966200
SamplesNA18533
Known GenesLINC01000
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614982
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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