A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331752



Internal ID20864919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:2185459..2190827hg38UCSC Ensembl
chr1:2116898..2122266hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg385369
hg195369
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057485
Samples
Known GenesC1orf86
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331752
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