A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6494426



Internal ID21151979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20904291..20958567hg38UCSC Ensembl
chr14:21372450..21426726hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3854277
hg1954277
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2044n223
Supporting Variantsnssv18016611
Samples
Known GenesECRP, RNASE2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6494426
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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