A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14289072



Internal ID22271862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155801625..155802005hg38UCSC Ensembl
chr1:155771416..155771796hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38381
hg19381
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3208076
Supporting Variants
SamplesNA19239
Known GenesGON4L
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14289072
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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