A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5436988



Internal ID215591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:175236608..175240324hg38UCSC Ensembl
chr2:176101336..176105052hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg383717
hg193717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16922339
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5436988
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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