A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508180



Internal ID20881479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66509215..66514556hg38UCSC Ensembl
chr15:66801553..66806894hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg385342
hg195342
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025418
Samples
Known GenesZWILCH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508180
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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