A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6494146



Internal ID21151699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:73704226..73704671hg38UCSC Ensembl
chr13:74278363..74278808hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg38446
hg19446
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18012588
Samples
Known GenesKLF12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6494146
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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