A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12819196



Internal ID6318897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66151382..66155221hg38UCSC Ensembl
Innerchr7:66151382..66155221hg38UCSC Ensembl
Outerchr7:66151137..66155450hg38UCSC Ensembl
chr7:65616369..65620208hg19UCSC Ensembl
Innerchr7:65616369..65620208hg19UCSC Ensembl
Outerchr7:65616124..65620437hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg383840
hg193840
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3613502
Supporting Variants
SamplesNA19917
Known GenesCRCP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12819196
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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