A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508911



Internal ID20882215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74013922..74017980hg38UCSC Ensembl
chr15:74306263..74310321hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg384059
hg194059
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026654
Samples
Known GenesPML
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508911
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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