A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18195260



Internal ID20762300
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 StatusS
Merged Variantsnsv6509608
Supporting Variants
Samples
Known GenesOCA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18195260
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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