A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327503



Internal ID20860642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:55170078..55170473hg38UCSC Ensembl
chr1:55635751..55636146hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38396
hg19396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062207
Samples
Known GenesUSP24
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327503
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