A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505253



Internal ID20878520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:97937611..97938227hg38UCSC Ensembl
chr14:98403948..98404564hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38617
hg19617
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022528
Samples
Known GenesC14orf64
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505253
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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