A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14322164



Internal ID22323466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95504264..95504648hg38UCSC Ensembl
chr5:94839968..94840352hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38385
hg19385
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3194405
Supporting Variants
SamplesNA19240
Known GenesTTC37
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14322164
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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