A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13515768



Internal ID4961145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72064216..72074787hg38UCSC Ensembl
chr9:74679132..74689703hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3810572
hg1910572
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620622
Supporting Variants
SamplesNA12842
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13515768
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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