A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3206085



Internal ID22354679
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14326631, nssv14326632
SamplesNA19238, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3206085
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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