A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16976434



Internal ID51680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:156657324..156666250hg38UCSC Ensembl
chr5:156084335..156093261hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg388927
hg198927
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6140964
Supporting Variants
Samples
Known GenesSGCD
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16976434
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.004381


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