A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3204259



Internal ID22353137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:154955392..154956340hg38UCSC Ensembl
chr6:155276526..155277474hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg38949
hg19949
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14331519, nssv14331520
SamplesNA19238, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3204259
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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