A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17633123



Internal ID21825170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:6491836..6491836hg38UCSC Ensembl
chr17:6395156..6395156hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6090063
Supporting Variants
Samples
Known GenesPITPNM3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17633123
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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