A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14326632



Internal ID22261193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6939147..6939446hg38UCSC Ensembl
chr6:6939380..6939679hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3206085
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14326632
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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