A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16964364



Internal ID43544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:37042182..37043277hg38UCSC Ensembl
chr5:37042284..37043379hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg381096
hg191096
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5457751
Supporting Variants
Samples
Known GenesNIPBL
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16964364
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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