A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17530968



Internal ID21855324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:34871120..34871120hg38UCSC Ensembl
chr1:35336721..35336721hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6041697
Supporting Variants
Samples
Known GenesDLGAP3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17530968
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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