A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331774



Internal ID20864941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:101041512..101042443hg38UCSC Ensembl
chr1:101507068..101507999hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg38932
hg19932
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200299
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331774
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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