A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16979724



Internal ID53862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177486764..177487060hg38UCSC Ensembl
chr5:176913765..176914061hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5458637
Supporting Variants
Samples
Known GenesPDLIM7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16979724
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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