A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15192516



Internal ID21331399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:40059014..40059014hg38UCSC Ensembl
chr1:40524686..40524686hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3951102
Supporting Variants
SamplesHG002
Known GenesCAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15192516
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