A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18201737



Internal ID20768777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:182027301..182032900hg38UCSC Ensembl
chr1:181996436..182002035hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg385600
hg195600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6329103
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18201737
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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