A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511083



Internal ID20884408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65345237..65346287hg38UCSC Ensembl
chr15:65637575..65638625hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg381051
hg191051
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025357
Samples
Known GenesIGDCC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511083
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