A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16977307



Internal ID52270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:154744630..154744938hg38UCSC Ensembl
chr5:154124190..154124498hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5469304
Supporting Variants
Samples
Known GenesLARP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16977307
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.159694


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