A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15177778



Internal ID21316574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:160535699..160535842hg38UCSC Ensembl
chr2:161392210..161392353hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3950793
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15177778
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