A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13456341



Internal ID6041646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33376726..33378928hg38UCSC Ensembl
Innerchr9:33376796..33378858hg38UCSC Ensembl
Outerchr9:33376656..33378998hg38UCSC Ensembl
chr9:33376724..33378926hg19UCSC Ensembl
Innerchr9:33376794..33378856hg19UCSC Ensembl
Outerchr9:33376654..33378996hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg382203
hg192203
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620322
Supporting Variants
SamplesNA19443
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13456341
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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