A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14312554



Internal ID22222423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:24902912..24903025hg38UCSC Ensembl
chr4:24904534..24904647hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3201739
Supporting Variants
SamplesHG00733
Known GenesCCDC149
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14312554
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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