A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5444856



Internal ID223220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:64075215..64084906hg38UCSC Ensembl
chr2:64302349..64312040hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg389692
hg199692
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16914983
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5444856
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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