A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477812



Internal ID21135365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:74561101..74561992hg38UCSC Ensembl
chr14:75027804..75028695hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38892
hg19892
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021476
Samples
Known GenesLTBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477812
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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