A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621952



Internal ID7008818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:134078320..134081892hg38UCSC Ensembl
Innerchr9:134078470..134081742hg38UCSC Ensembl
Outerchr9:134078170..134082042hg38UCSC Ensembl
chr9:136943442..136947014hg19UCSC Ensembl
Innerchr9:136943592..136946864hg19UCSC Ensembl
Outerchr9:136943292..136947164hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg383573
hg193573
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13641408, essv13641409
SamplesNA19098, HG02561
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621952
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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