A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614160



Internal ID6654367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:93453076..93457978hg38UCSC Ensembl
Innerchr7:93453076..93457978hg38UCSC Ensembl
Outerchr7:93452862..93458221hg38UCSC Ensembl
chr7:93082388..93087290hg19UCSC Ensembl
Innerchr7:93082388..93087290hg19UCSC Ensembl
Outerchr7:93082174..93087533hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg384903
hg194903
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12890837
SamplesNA19676
Known GenesCALCR
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614160
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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