A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18188579



Internal ID20755619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34309901..34595700hg38UCSC Ensembl
chr15:34602102..34887901hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38285800
hg19285800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6499953
Supporting Variants
Samples
Known GenesGOLGA8A, GOLGA8B, LPCAT4, MIR1233-1, MIR1233-2, NOP10, NUTM1, SLC12A6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18188579
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00049


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