A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15176382



Internal ID21315178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58710716..58710802hg38UCSC Ensembl
chr16:58744620..58744706hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3945931
Supporting Variants
SamplesHG002
Known GenesGOT2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15176382
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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