A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321861



Internal ID20854969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:195735601..195790400hg38UCSC Ensembl
chr1:195704731..195759530hg19UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg3854800
hg1954800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202008
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321861
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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