A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498036



Internal ID20871244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90639492..90649125hg38UCSC Ensembl
chr15:91182724..91192356hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg389634
hg199633
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196896
Samples
Known GenesCRTC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498036
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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