A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320699



Internal ID20853800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:198256457..198256892hg38UCSC Ensembl
chr1:198225587..198226022hg19UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg38436
hg19436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18056211
Samples
Known GenesNEK7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320699
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