A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512753



Internal ID20886091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68234876..68238187hg38UCSC Ensembl
chr15:68527214..68530525hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg383312
hg193312
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026252
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512753
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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