A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621514



Internal ID6661693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112423996..112435831hg38UCSC Ensembl
Innerchr9:112424496..112435331hg38UCSC Ensembl
Outerchr9:112422996..112436831hg38UCSC Ensembl
chr9:115186276..115198111hg19UCSC Ensembl
Innerchr9:115186776..115197611hg19UCSC Ensembl
Outerchr9:115185276..115199111hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3811836
hg1911836
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13606205, essv13606206
SamplesHG01810, NA18571
Known GenesHSDL2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621514
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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