A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610346



Internal ID20983417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:136434383..136440366hg38UCSC Ensembl
chr6:136755521..136761504hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg385984
hg195984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140126
Samples
Known GenesMAP7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610346
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