A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5422727



Internal ID201764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150318621..150321161hg38UCSC Ensembl
chr1:150291068..150293609hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg382541
hg192542
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16890551
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5422727
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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