A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004599



Internal ID21913942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:60613464..60613632hg38UCSC Ensembl
chr9_gl000199_random:94906..95074hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17590304
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004599
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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