A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620499



Internal ID7007370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:61660998..61699030hg38UCSC Ensembl
chr9:44868836..44906868hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3838033
hg1938033
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13491716, essv13491714, essv13491717, essv13491715, essv13491718
SamplesNA20878, HG03667, HG00129, HG03779, HG02760
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620499
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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