A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499908



Internal ID20873133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68792878..68793770hg38UCSC Ensembl
chr15:69085217..69086109hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38893
hg19893
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026279
Samples
Known GenesANP32A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499908
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