A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13516174



Internal ID6967942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72370141..72377646hg38UCSC Ensembl
chr9:74985057..74992562hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg387506
hg197506
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620634
Supporting Variants
SamplesNA21143
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13516174
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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