A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368334



Internal ID21025887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:14135544..14136173hg38UCSC Ensembl
chr4:14137168..14137797hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg38630
hg19630
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18108174
Samples
Known GenesLINC01085
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368334
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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