A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13626277



Internal ID2338261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129234009..129245144hg38UCSC Ensembl
Innerchr9:129234029..129245124hg38UCSC Ensembl
Outerchr9:129233989..129245164hg38UCSC Ensembl
chr9:131996288..132007423hg19UCSC Ensembl
Innerchr9:131996308..132007403hg19UCSC Ensembl
Outerchr9:131996268..132007443hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3811136
hg1911136
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621826
Supporting Variants
SamplesHG02078
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13626277
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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