A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17000009



Internal ID67586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73677555..73681259hg38UCSC Ensembl
chr7:73091885..73095589hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg383705
hg193705
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5480906
Supporting Variants
Samples
Known GenesDNAJC30
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17000009
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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