A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513538



Internal ID20886883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:96172422..96176284hg38UCSC Ensembl
chr14:96638759..96642621hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg383863
hg193863
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022234
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513538
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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