A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526524



Internal ID22395904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:24964831..24965505hg38UCSC Ensembl
chr4:24966453..24967127hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38675
hg19675
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14312555, nssv14312556, nssv14312558, nssv14312557
SamplesHG00512, NA19239, NA19240, HG00513
Known GenesCCDC149
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526524
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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