A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5444185



Internal ID222565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:71260031..71260917hg38UCSC Ensembl
chr2:71487161..71488047hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg38887
hg19887
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16916073
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5444185
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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