A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12709413



Internal ID4260456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:25270050..25275326hg38UCSC Ensembl
Innerchr7:25270071..25275306hg38UCSC Ensembl
Outerchr7:25270030..25275347hg38UCSC Ensembl
chr7:25309669..25314945hg19UCSC Ensembl
Innerchr7:25309690..25314925hg19UCSC Ensembl
Outerchr7:25309649..25314966hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg385277
hg195277
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3612596
Supporting Variants
SamplesHG03829
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12709413
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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