A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321832



Internal ID20854940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:91660756..91675854hg38UCSC Ensembl
chr1:92126313..92141411hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg3815099
hg1915099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203164
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321832
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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