A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17358218



Internal ID22583887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156702190..156702933hg38UCSC Ensembl
chr1:156671982..156672725hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg38744
hg19744
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5870783
Supporting Variants
Samples
Known GenesCRABP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17358218
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