A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329623



Internal ID20862776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150482081..150482631hg38UCSC Ensembl
chr1:150454557..150455107hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38551
hg19551
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201522
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329623
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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