A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500897



Internal ID20874127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:99537905..99549999hg38UCSC Ensembl
chr14:100004242..100016336hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3812095
hg1912095
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184480
Samples
Known GenesCCDC85C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500897
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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