A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12685802



Internal ID4943682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:14996902..15081927hg38UCSC Ensembl
chr7:15036527..15121552hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3885026
hg1985026
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3612331
Supporting Variants
SamplesNA12813
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12685802
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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