A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5416740



Internal ID195957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:43938442..43938542hg38UCSC Ensembl
chr1:44404114..44404214hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16902542
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5416740
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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