A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18021383



Internal ID20588423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:81176471..81176965hg38UCSC Ensembl
chr14:81642815..81643309hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg38495
hg19495
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6486273
Supporting Variants
Samples
Known GenesGTF2A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18021383
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00052


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