A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17361571



Internal ID22587240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:30773220..30773441hg38UCSC Ensembl
chr1:31246067..31246288hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg38222
hg19222
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5887081
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17361571
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