A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15192044



Internal ID21330913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8912172..8912172hg38UCSC Ensembl
chr1:8972231..8972231hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg38412
hg19412
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3941302
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15192044
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