A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505170



Internal ID20878436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:22965199..22967177hg38UCSC Ensembl
chr15:22905891..22907869hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381979
hg191979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022797
Samples
Known GenesCYFIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505170
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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