A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319238



Internal ID20852330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:48467701..48475600hg38UCSC Ensembl
chr1:48933373..48941272hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg387900
hg197900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201412
Samples
Known GenesSPATA6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319238
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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