A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5438950



Internal ID217500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:219840235..219864346hg38UCSC Ensembl
chr1:220013577..220037688hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3824112
hg1924112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16897175
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5438950
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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