A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13270



Internal ID15831647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26883977..26905128hg38UCSC Ensembl
Outerchr6:26883163..26905265hg38UCSC Ensembl
Innerchr6:26851756..26872907hg19UCSC Ensembl
Outerchr6:26850942..26873044hg19UCSC Ensembl
Innerchr6:26959735..26980886hg18UCSC Ensembl
Outerchr6:26958921..26981023hg18UCSC Ensembl
Innerchr6:26959735..26980886hg17UCSC Ensembl
Outerchr6:26958921..26981023hg17UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3822103
hg1922103
hg1822103
hg1722103
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv10806
Supporting Variants
SamplesNA12802
Known GenesGUSBP2
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)nssv13270
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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