A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490122



Internal ID21147675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21195207..21200304hg38UCSC Ensembl
chr14:21663366..21668463hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg385098
hg195098
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016641
Samples
Known GenesLINC00641
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490122
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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