A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513535



Internal ID20886880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:91962793..91969021hg38UCSC Ensembl
chr14:92429137..92435365hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg386229
hg196229
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195289
Samples
Known GenesTRIP11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513535
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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