A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509814



Internal ID20883126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90726525..90728580hg38UCSC Ensembl
chr15:91269756..91271811hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg382056
hg192056
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027387
Samples
Known GenesBLM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509814
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