A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011624



Internal ID21920967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:26048866..26251689hg38UCSC Ensembl
chr9:26048864..26251687hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38202824
hg19202824
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593024
Samples
Known GenesLOC100506422
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011624
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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