A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5458637



Internal ID236657
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 StatusM
Merged Variants
Supporting Variantsnssv16979724
Samples
Known GenesPDLIM7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5458637
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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