A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5425649



Internal ID204606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:81155809..81155904hg38UCSC Ensembl
chr1:81621494..81621589hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16905436
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5425649
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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