A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196140



Internal ID20763180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:56105101..56109900hg38UCSC Ensembl
chr15:56397299..56402098hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg384800
hg194800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6509917
Supporting Variants
Samples
Known GenesRFX7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196140
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00087


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