A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316782



Internal ID20849864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:158519625..158923788hg38UCSC Ensembl
chr1:158489415..158893578hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg38404164
hg19404164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053048
Samples
Known GenesMNDA, OR10X1, OR10Z1, OR6K2, OR6K3, OR6K6, OR6N1, OR6N2, OR6P1, OR6Y1, SPTA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316782
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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