A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16968752



Internal ID46490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:87118336..87122589hg38UCSC Ensembl
chr5:86414153..86418406hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg384254
hg194254
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5466762
Supporting Variants
Samples
Known GenesLOC101929380
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16968752
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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