A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5432631



Internal ID211369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:43641835..43647835hg38UCSC Ensembl
chr1:44107506..44113506hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg386001
hg196001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16901576
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5432631
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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