A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509427



Internal ID20882736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49424723..49425119hg38UCSC Ensembl
chr15:49716920..49717316hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38397
hg19397
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024783
Samples
Known GenesFAM227B, FGF7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509427
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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