A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5883692



Internal ID22658674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:40480325..40480423hg38UCSC Ensembl
chr1:40945997..40946095hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17377242
Samples
Known GenesZFP69
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5883692
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