A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18204421



Internal ID20771461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:75038212..75041347hg38UCSC Ensembl
chr1:75503896..75507031hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg383136
hg193136
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6327188
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18204421
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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