A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511767



Internal ID20885097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90712709..90722896hg38UCSC Ensembl
chr15:91255940..91266127hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3810188
hg1910188
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027386
Samples
Known GenesBLM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511767
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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