A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326513



Internal ID20859649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23076791..23096802hg38UCSC Ensembl
chr1:23403284..23423295hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3820012
hg1920012
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202771
Samples
Known GenesKDM1A, LUZP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326513
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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