A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17537638



Internal ID21861993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:36956737..36956825hg38UCSC Ensembl
chr5:36956839..36956927hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5999700
Supporting Variants
Samples
Known GenesNIPBL
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17537638
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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