A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14329800



Internal ID22264543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158704805..158705057hg38UCSC Ensembl
chr6:159125837..159126089hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38253
hg19253
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3202704
Supporting Variants
SamplesNA19238
Known GenesSYTL3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14329800
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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