A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177290



Internal ID20744330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:23561301..23568300hg38UCSC Ensembl
chr15:23806448..23813447hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg387000
hg197000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6495982
Supporting Variants
Samples
Known GenesMIR4508, MKRN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177290
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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