A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325716



Internal ID20858848
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 StatusM
Merged Variantsdgv4n223
Supporting Variantsnssv18204465
Samples
Known GenesFAM41C, FAM87B, LINC00115, LINC01128
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325716
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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