A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14329408



Internal ID22144273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73559736..73560177hg38UCSC Ensembl
chr6:74269459..74269900hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38442
hg19442
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3204492
Supporting Variants
SamplesHG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14329408
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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