A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322577



Internal ID20855690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:244824224..244835080hg38UCSC Ensembl
chr1:244987526..244998382hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3810857
hg1910857
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200669
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322577
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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