A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6476677



Internal ID21134230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:74046986..74683263hg38UCSC Ensembl
chr13:74621123..75257400hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg38636278
hg19636278
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196657
Samples
Known GenesKLF12, LINC00347, LINC00381
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6476677
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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