A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17480865



Internal ID22538769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:85696910..85710914hg38UCSC Ensembl
chr1:86162593..86176597hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg3814005
hg1914005
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5830824
Supporting Variants
Samples
Known GenesZNHIT6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17480865
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