A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18021762



Internal ID20588802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:85384358..85432941hg38UCSC Ensembl
chr14:85850702..85899285hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3848584
hg1948584
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6488071
Supporting Variants
Samples
Known GenesLINC00911
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18021762
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00015


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