A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17518862



Internal ID21843221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:31203650..31203745hg38UCSC Ensembl
chr1:31676497..31676592hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5983922
Supporting Variants
Samples
Known GenesNKAIN1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17518862
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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