A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6483269



Internal ID21140822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:52651301..52662900hg38UCSC Ensembl
chr14:53118019..53129618hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg3811600
hg1911600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020010
Samples
Known GenesERO1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6483269
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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