A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12709435



Internal ID6726292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:25663322..25743431hg38UCSC Ensembl
chr7:25702942..25783051hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3880110
hg1980110
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3612608
Supporting Variants
SamplesNA20853
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12709435
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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