A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6491165



Internal ID21148718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:82918679..83057238hg38UCSC Ensembl
chr14:83385023..83523582hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg38138560
hg19138560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021511
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6491165
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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