A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14331426



Internal ID22329301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:153235975..153244016hg38UCSC Ensembl
chr6:153557110..153565151hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg388042
hg198042
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3206420
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14331426
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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