A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202097



Internal ID20769138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:59293901..59298400hg38UCSC Ensembl
chr1:59759573..59764072hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg384500
hg194500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6324341
Supporting Variants
Samples
Known GenesFGGY
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202097
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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