A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004033



Internal ID21913376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:9520039..9520142hg38UCSC Ensembl
chr6:9520272..9520375hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17562429
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004033
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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