A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003540



Internal ID21912883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:67855860..67855931hg38UCSC Ensembl
chr9:44121970..44122026hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3872
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17594081
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003540
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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