A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13433602



Internal ID4931036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:27030398..27032773hg38UCSC Ensembl
Innerchr9:27030398..27032773hg38UCSC Ensembl
Outerchr9:27030157..27032904hg38UCSC Ensembl
chr9:27030396..27032771hg19UCSC Ensembl
Innerchr9:27030396..27032771hg19UCSC Ensembl
Outerchr9:27030155..27032902hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg382376
hg192376
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620122
Supporting Variants
SamplesNA12775
Known GenesIFT74
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13433602
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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