A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16949202



Internal ID33486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:61749453..61765610hg38UCSC Ensembl
chr4:62615171..62631328hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3816158
hg1916158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5469403
Supporting Variants
Samples
Known GenesLPHN3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16949202
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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