A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332167



Internal ID20865336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150131486..150131807hg38UCSC Ensembl
chr1:150103641..150103968hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg38322
hg19328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052944
Samples
Known GenesVPS45
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332167
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