A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489010



Internal ID21146563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:51356095..51425247hg38UCSC Ensembl
chr14:51822813..51891965hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg3869153
hg1969153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18019140
Samples
Known GenesLINC00640
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489010
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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