A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512932



Internal ID20886272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69567796..69586966hg38UCSC Ensembl
chr15:69860135..69879305hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3819171
hg1919171
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182765
Samples
Known GenesLOC145837
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512932
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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