A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012417



Internal ID21921760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73442791..73443431hg38UCSC Ensembl
chr6:74152514..74153154hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38641
hg19641
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17568313
Samples
Known GenesMB21D1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012417
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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