A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6318006



Internal ID20851097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:197169695..197170280hg38UCSC Ensembl
chr1:197138825..197139410hg19UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg38586
hg19586
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18056390
Samples
Known GenesZBTB41
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6318006
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