A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497809



Internal ID20871017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64367296..64376145hg38UCSC Ensembl
chr15:64659495..64668344hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg388850
hg198850
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177580
Samples
Known GenesKIAA0101
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497809
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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