A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17441594



Internal ID22499464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3957769..3961362hg38UCSC Ensembl
chr6:3958003..3961596hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg383594
hg193594
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5896921
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17441594
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