A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15178268



Internal ID21317064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:25634203..25634252hg38UCSC Ensembl
chr2:25857072..25857121hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3929981
Supporting Variants
SamplesHG002
Known GenesDTNB
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15178268
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