A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513653



Internal ID20886999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80911976..80913529hg38UCSC Ensembl
chr15:81204317..81205870hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg381554
hg191554
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191256
Samples
Known GenesKIAA1199
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513653
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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