A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17619085



Internal ID21811132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:1549105..1549174hg38UCSC Ensembl
chr17:1452399..1452468hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6031711
Supporting Variants
Samples
Known GenesPITPNA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17619085
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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