A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327483



Internal ID20860622
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 StatusM
Merged Variants
Supporting Variantsnssv18062462
Samples
Known GenesNOL9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327483
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