A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486425



Internal ID21143978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21256233..21259946hg38UCSC Ensembl
chr14:21724392..21728105hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg383714
hg193714
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016650
Samples
Known GenesHNRNPC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486425
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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