A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15034



Internal ID15828634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:159666205..159666879hg38UCSC Ensembl
Outerchr6:159664365..159668231hg38UCSC Ensembl
Innerchr6:160087237..160087911hg19UCSC Ensembl
Outerchr6:160085397..160089263hg19UCSC Ensembl
Innerchr6:160007227..160007901hg18UCSC Ensembl
Outerchr6:160005387..160009253hg18UCSC Ensembl
Innerchr6:160057648..160058322hg17UCSC Ensembl
Outerchr6:160055808..160059674hg17UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg383867
hg193867
hg183867
hg173867
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7983
Supporting Variants
SamplesNA10839
Known Genes
MethodOligo aCGH
AnalysisStatistical threshold = 5.0, minimum +/- log2 ratio = 0.25 and minimum number of probes = 2
PlatformAgilent-015686 Custom Human 244K CGH Microarray
Comments
ReferencePerry_et_al_2008
Pubmed ID18304495
Accession Number(s)nssv15034
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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