A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509608



Internal ID20882919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:27770994..27771074hg38UCSC Ensembl
chr15:28016140..28016220hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195260
Samples
Known GenesOCA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509608
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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