A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5870019



Internal ID22644954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151318147..151318440hg38UCSC Ensembl
chr1:151290623..151290916hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38294
hg19294
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17365710
Samples
Known GenesPI4KB
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5870019
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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