A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486760



Internal ID21144313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:22953792..22954866hg38UCSC Ensembl
chr14:23423001..23424075hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg381075
hg191075
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016715
Samples
Known GenesHAUS4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486760
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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