A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499877



Internal ID20873102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77415201..77419600hg38UCSC Ensembl
chr15:77707543..77711942hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg384400
hg194400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178088
Samples
Known GenesPEAK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499877
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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