A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325954



Internal ID20859088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:178940457..179040271hg38UCSC Ensembl
chr1:178909592..179009406hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3899815
hg1999815
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201692
Samples
Known GenesFAM20B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325954
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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