A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14314862



Internal ID22284428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37037170..37037239hg38UCSC Ensembl
chr4:37038792..37038861hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3197065
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14314862
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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