A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5442064



Internal ID220507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:159766505..159766577hg38UCSC Ensembl
chr2:160623016..160623088hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16921365
Samples
Known GenesMARCH7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5442064
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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