A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17565519



Internal ID21757484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:14212238..14212238hg38UCSC Ensembl
chr7:14251863..14251863hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg38796
hg19796
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6077057
Supporting Variants
Samples
Known GenesDGKB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17565519
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