A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6369154



Internal ID9539776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:66218621..66238391hg38UCSC Ensembl
Outerchr7:66218464..66238544hg38UCSC Ensembl
Innerchr7:65683608..65703378hg19UCSC Ensembl
Outerchr7:65683451..65703531hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg3820081
hg1920081
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2677943
Supporting Variants
SamplesNA19070
Known GenesTPST1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6369154
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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