A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326275



Internal ID20859409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:3520899..3569290hg38UCSC Ensembl
chr1:3437463..3485854hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3848392
hg1948392
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202423
Samples
Known GenesMEGF6, MIR551A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326275
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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