A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13606226



Internal ID3608043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112530526..112531644hg38UCSC Ensembl
Innerchr9:112530571..112531600hg38UCSC Ensembl
Outerchr9:112530482..112531689hg38UCSC Ensembl
chr9:115292806..115293924hg19UCSC Ensembl
Innerchr9:115292851..115293880hg19UCSC Ensembl
Outerchr9:115292762..115293969hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg381119
hg191119
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621516
Supporting Variants
SamplesNA19682
Known GenesKIAA1958
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13606226
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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