A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17450432



Internal ID22508302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:244731665..244736307hg38UCSC Ensembl
chr1:244894967..244899609hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg384643
hg194643
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5829295
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17450432
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