A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186536



Internal ID20753576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67514501..67526400hg38UCSC Ensembl
chr15:67806839..67818738hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3811900
hg1911900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6504308
Supporting Variants
Samples
Known GenesC15orf61, IQCH-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186536
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00013


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