A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616030



Internal ID20989101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:125917997..125919581hg38UCSC Ensembl
chr6:126239143..126240727hg19UCSC Ensembl
Cytoband6q22.32
Allele length
AssemblyAllele length
hg381585
hg191585
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18138702
Samples
Known GenesNCOA7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616030
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