A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486273



Internal ID21143826
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 StatusM
Merged Variants
Supporting Variantsnssv18021383
Samples
Known GenesGTF2A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486273
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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