A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5870596



Internal ID22645532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:14867634..14874886hg38UCSC Ensembl
chr1:15194130..15201382hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg387253
hg197253
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17366558
Samples
Known GenesKAZN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5870596
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer