A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6485787



Internal ID21143340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:59559541..59560183hg38UCSC Ensembl
chr14:60026259..60026901hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38643
hg19643
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020430
Samples
Known GenesCCDC175
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6485787
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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