A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620602



Internal ID7007472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:71185488..71242459hg38UCSC Ensembl
chr9:73800404..73857375hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg3856972
hg1956972
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13513850
SamplesHG04023
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620602
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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