A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5436774



Internal ID215382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:149575614..149575703hg38UCSC Ensembl
chr2:150432128..150432217hg19UCSC Ensembl
Cytoband2q23.2
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16920514
Samples
Known GenesMMADHC
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5436774
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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