A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12916095



Internal ID647632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:106063117..106066356hg38UCSC Ensembl
Innerchr7:106063117..106066356hg38UCSC Ensembl
Outerchr7:106062941..106066507hg38UCSC Ensembl
chr7:105703563..105706802hg19UCSC Ensembl
Innerchr7:105703563..105706802hg19UCSC Ensembl
Outerchr7:105703387..105706953hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg383240
hg193240
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3614437
Supporting Variants
SamplesHG00284
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12916095
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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