A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527938



Internal ID22397324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15726396..15726485hg38UCSC Ensembl
chr6:15726627..15726716hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14327549, nssv14327551, nssv14327548, nssv14327552, nssv14327550
SamplesNA19238, NA19239, HG00732, NA19240, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527938
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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