A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512207



Internal ID20885539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67373059..67373650hg38UCSC Ensembl
chr15:67665397..67665988hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38592
hg19592
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025458
Samples
Known GenesIQCH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512207
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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