A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003632



Internal ID21912975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:43905004..43905239hg38UCSC Ensembl
chr6:43872741..43872976hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38236
hg19236
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576377
Samples
Known GenesLOC100132354
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003632
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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