A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16909609



Internal ID7181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:4633904..4634319hg38UCSC Ensembl
chr2:4681494..4681909hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg38416
hg19416
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5436912
Supporting Variants
Samples
Known GenesLOC727982
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16909609
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.004059


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