A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14313221



Internal ID22280846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:27246369..27246754hg38UCSC Ensembl
chr4:27247991..27248376hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38386
hg19386
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3204115
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14313221
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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