A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621513



Internal ID6661692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112415565..112463028hg38UCSC Ensembl
Innerchr9:112415573..112463020hg38UCSC Ensembl
Outerchr9:112415557..112463036hg38UCSC Ensembl
chr9:115177845..115225308hg19UCSC Ensembl
Innerchr9:115177853..115225300hg19UCSC Ensembl
Outerchr9:115177837..115225316hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3847464
hg1947464
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13606204
SamplesHG01810
Known GenesHSDL2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621513
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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