A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17562209



Internal ID21886564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149786015..149786144hg38UCSC Ensembl
chr6:150107151..150107280hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6013426
Supporting Variants
Samples
Known GenesPCMT1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17562209
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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