A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17415962



Internal ID22473832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:178076060..178151307hg38UCSC Ensembl
chr5:177503061..177578308hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3875248
hg1975248
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5901935
Supporting Variants
Samples
Known GenesN4BP3, NHP2, RMND5B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17415962
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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