A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18145185



Internal ID20712225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:75169627..75170017hg38UCSC Ensembl
chr6:75879343..75879733hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38391
hg19391
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6413738
Supporting Variants
Samples
Known GenesCOL12A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18145185
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00073


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