A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18201438



Internal ID20768478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:50955001..50965700hg38UCSC Ensembl
chr1:51420673..51431372hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg3810700
hg1910700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6326302
Supporting Variants
Samples
Known GenesFAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18201438
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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