A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510384



Internal ID20883702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78079001..78085900hg38UCSC Ensembl
chr15:78371343..78378242hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg386900
hg196900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026751
Samples
Known GenesMIR5003
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510384
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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