A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12709419



Internal ID6455637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:25358871..25376571hg38UCSC Ensembl
Innerchr7:25359371..25376071hg38UCSC Ensembl
Outerchr7:25357871..25377571hg38UCSC Ensembl
chr7:25398490..25416190hg19UCSC Ensembl
Innerchr7:25398990..25415690hg19UCSC Ensembl
Outerchr7:25397490..25417190hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3817701
hg1917701
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3612599
Supporting Variants
SamplesNA20514
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12709419
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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