A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16975911



Internal ID51337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:156942071..156944576hg38UCSC Ensembl
chr5:156369082..156371587hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg382506
hg192506
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5472443
Supporting Variants
Samples
Known GenesTIMD4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16975911
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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