A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18051670



Internal ID20618710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:114902452..114902814hg38UCSC Ensembl
chr1:115445073..115445435hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg38363
hg19363
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6324523
Supporting Variants
Samples
Known GenesSYCP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18051670
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.02761


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