A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6494037



Internal ID21151590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:30481409..30481878hg38UCSC Ensembl
chr14:30950615..30951084hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38470
hg19470
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18017660
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6494037
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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