A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322637



Internal ID20855750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:64983991..64984698hg38UCSC Ensembl
chr1:65449674..65450381hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38708
hg19708
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204290
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322637
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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