A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17469533



Internal ID22527423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:31349919..31361538hg38UCSC Ensembl
chr1:31822766..31834385hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg3811620
hg1911620
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5829985
Supporting Variants
Samples
Known GenesZCCHC17
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17469533
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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