A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508800



Internal ID20882104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:73225980..73226292hg38UCSC Ensembl
chr15:73518321..73518633hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026628
Samples
Known GenesNEO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508800
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