A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4391201



Internal ID21382231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:99577303..99577454hg38UCSC Ensembl
chr14:100043640..100043791hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15705836
Samples
Known GenesCCDC85C
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4391201
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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