A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514353



Internal ID20887706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:73562160..73562887hg38UCSC Ensembl
chr15:73854501..73855228hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38728
hg19728
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026643
Samples
Known GenesNPTN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514353
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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