A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019987



Internal ID21929330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63392892..63397490hg38UCSC Ensembl
chr6:64102797..64107395hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg384599
hg194599
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576266
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019987
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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