A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18062462



Internal ID20629502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6540116..6541278hg38UCSC Ensembl
chr1:6600176..6601338hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg381163
hg191163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6327483
Supporting Variants
Samples
Known GenesNOL9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18062462
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer