A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621543



Internal ID6661721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113366366..113368577hg38UCSC Ensembl
Innerchr9:113366366..113368577hg38UCSC Ensembl
Outerchr9:113366277..113368848hg38UCSC Ensembl
chr9:116128646..116130857hg19UCSC Ensembl
Innerchr9:116128646..116130857hg19UCSC Ensembl
Outerchr9:116128557..116131128hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg382212
hg192212
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13606766
SamplesNA18631
Known GenesBSPRY
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621543
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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