A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512672



Internal ID20886009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:96675082..97083345hg38UCSC Ensembl
chr15:97218312..97626575hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38408264
hg19408264
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180296
Samples
Known GenesSPATA8, SPATA8-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512672
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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