A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499998



Internal ID20873223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75707845..75710558hg38UCSC Ensembl
chr15:76000186..76002899hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg382714
hg192714
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025738
Samples
Known GenesCSPG4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499998
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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