A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012006



Internal ID21921349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:178261126..178263045hg38UCSC Ensembl
chr5:177688127..177690046hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg381920
hg191920
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17566252
Samples
Known GenesCOL23A1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012006
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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