A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621899



Internal ID7008765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:131781647..131788081hg38UCSC Ensembl
Innerchr9:131781647..131788081hg38UCSC Ensembl
Outerchr9:131781401..131788346hg38UCSC Ensembl
chr9:134657034..134663468hg19UCSC Ensembl
Innerchr9:134657034..134663468hg19UCSC Ensembl
Outerchr9:134656788..134663733hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg386435
hg196435
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13633346, essv13633345
SamplesHG00640, HG02232
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621899
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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