A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500880



Internal ID20874110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:22977060..22982705hg38UCSC Ensembl
chr15:22890363..22896008hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg385646
hg195646
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022800
Samples
Known GenesCYFIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500880
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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