A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18204465



Internal ID20771505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:785093..906521hg38UCSC Ensembl
chr1:720473..841901hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38121429
hg19121429
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6325716
Supporting Variants
Samples
Known GenesFAM41C, FAM87B, LINC00115, LINC01128
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18204465
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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