A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504626



Internal ID20877888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72279401..72281600hg38UCSC Ensembl
chr15:72571742..72573941hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2579n223
Supporting Variantsnssv18026576
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504626
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