A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6492506



Internal ID21150059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:71525240..71557975hg38UCSC Ensembl
chr14:71991957..72024692hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3832736
hg1932736
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021020
Samples
Known GenesSIPA1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6492506
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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