A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508069



Internal ID20881367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:87166366..87311395hg38UCSC Ensembl
chr15:87709597..87854626hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38145030
hg19145030
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2621n223
Supporting Variantsnssv18179689
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508069
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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