A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332593



Internal ID20865766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:160028248..160029109hg38UCSC Ensembl
chr1:159998038..159998899hg19UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg38862
hg19862
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052439
Samples
Known GenesPIGM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332593
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