A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5902584



Internal ID22677744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:170274293..170534408hg38UCSC Ensembl
chr5:169701297..169961412hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg38260116
hg19260116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17411877
Samples
Known GenesKCNIP1, KCNMB1, LCP2, LOC257358
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5902584
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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