A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18188192



Internal ID20755232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:96329501..96335300hg38UCSC Ensembl
chr15:96872730..96878529hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg385800
hg195800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6513896
Supporting Variants
Samples
Known GenesMIR1469, NR2F2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18188192
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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