A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335238



Internal ID20868430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:185161901..185171800hg38UCSC Ensembl
chr1:185131033..185140932hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg389900
hg199900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18054465
Samples
Known GenesSWT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335238
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