A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6402973



Internal ID21060526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:17110607..17112574hg38UCSC Ensembl
chr6:17110838..17112805hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg381968
hg191968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143237
Samples
Known GenesSTMND1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6402973
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