A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320534



Internal ID20853633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23003588..23030612hg38UCSC Ensembl
chr1:23330081..23357105hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3827025
hg1927025
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202349
Samples
Known GenesC1orf234, KDM1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320534
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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