A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507600



Internal ID20880894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49434780..49443813hg38UCSC Ensembl
chr15:49726977..49736010hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg389034
hg199034
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024668
Samples
Known GenesFAM227B, FGF7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507600
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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