A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13493767



Internal ID1025027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:43052167..43075523hg38UCSC Ensembl
chr9:66243042..66266398hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3823357
hg1923357
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620507
Supporting Variants
SamplesHG00641
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13493767
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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