A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332448



Internal ID20865620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:92631120..92632829hg38UCSC Ensembl
chr1:93096677..93098386hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg381710
hg191710
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065198
Samples
Known GenesEVI5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332448
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