A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508468



Internal ID20881769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49615932..49622878hg38UCSC Ensembl
chr15:49908129..49915075hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg386947
hg196947
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024696
Samples
Known GenesDTWD1, FAM227B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508468
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