A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6005126



Internal ID21914469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:62794461..62939979hg38UCSC Ensembl
chr6:63504366..63649884hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38145519
hg19145519
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563475
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6005126
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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