A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620711



Internal ID7007581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:74916363..74939312hg38UCSC Ensembl
chr9:77531279..77554228hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3822950
hg1922950
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13526556, essv13526557
SamplesHG02973, NA18504
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620711
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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