A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12917586



Internal ID6301805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:106427906..106430734hg38UCSC Ensembl
Innerchr7:106427925..106430715hg38UCSC Ensembl
Outerchr7:106427887..106430753hg38UCSC Ensembl
chr7:106068352..106071180hg19UCSC Ensembl
Innerchr7:106068371..106071161hg19UCSC Ensembl
Outerchr7:106068333..106071199hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg382829
hg192829
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3614444
Supporting Variants
SamplesNA19904
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12917586
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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