A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17427733



Internal ID22485603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:140404028..140415009hg38UCSC Ensembl
chr6:140725165..140736146hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3810982
hg1910982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5899086
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17427733
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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