A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12715689



Internal ID3489261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:28910998..28911779hg38UCSC Ensembl
Innerchr7:28911012..28911766hg38UCSC Ensembl
Outerchr7:28910985..28911793hg38UCSC Ensembl
chr7:28950615..28951396hg19UCSC Ensembl
Innerchr7:28950629..28951383hg19UCSC Ensembl
Outerchr7:28950602..28951410hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38782
hg19782
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3612678
Supporting Variants
SamplesHG03099
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12715689
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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