A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6491914



Internal ID21149467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:36506958..36507795hg38UCSC Ensembl
chr14:36976163..36977000hg19UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg38838
hg19838
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18017967
Samples
Known GenesSFTA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6491914
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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