A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6600797



Internal ID20973868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149921947..150024548hg38UCSC Ensembl
chr6:150243083..150345684hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38102602
hg19102602
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217094
Samples
Known GenesRAET1G, RAET1K, RAET1L, ULBP1, ULBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6600797
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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