A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326246



Internal ID20859380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:81261881..81298917hg38UCSC Ensembl
chr1:81727566..81764602hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3837037
hg1937037
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205102
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326246
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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