A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18201069



Internal ID20768109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:175317101..175345000hg38UCSC Ensembl
chr1:175286237..175314136hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg3827900
hg1927900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6329720
Supporting Variants
Samples
Known GenesTNR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18201069
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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