A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17574497



Internal ID21766540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149759148..149759765hg38UCSC Ensembl
chr6:150080284..150080901hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38618
hg19618
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6005904
Supporting Variants
Samples
Known GenesPCMT1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17574497
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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