A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6039201



Internal ID21948544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:64914791..64915021hg38UCSC Ensembl
chr14:65381509..65381739hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg38231
hg19231
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17605362
Samples
Known GenesCHURC1, CHURC1-FNTB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6039201
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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