A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15185522



Internal ID21324334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:110310153..110310153hg38UCSC Ensembl
chr1:110852775..110852775hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3936459
Supporting Variants
SamplesHG002
Known GenesLOC440600
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15185522
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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