A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605787



Internal ID20978858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:133993002..133993400hg38UCSC Ensembl
chr6:134314140..134314538hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg38399
hg19399
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139408
Samples
Known GenesSLC2A12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605787
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