A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5441029



Internal ID219517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:36373902..36375553hg38UCSC Ensembl
chr2:36601045..36602696hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg381652
hg191652
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16912158
Samples
Known GenesCRIM1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5441029
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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