A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331244



Internal ID20864406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:59319562..59367320hg38UCSC Ensembl
chr1:59785234..59832992hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg3847759
hg1947759
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061952
Samples
Known GenesFGGY
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331244
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