A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16710



Internal ID15497521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31899962..31903219hg38UCSC Ensembl
Outerchr6:31898992..31903913hg38UCSC Ensembl
Innerchr6:31867739..31870996hg19UCSC Ensembl
Outerchr6:31866769..31871690hg19UCSC Ensembl
Innerchr6:31975718..31978975hg18UCSC Ensembl
Outerchr6:31974748..31979669hg18UCSC Ensembl
Innerchr6:31975718..31978975hg17UCSC Ensembl
Outerchr6:31974748..31979669hg17UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg384922
hg194922
hg184922
hg174922
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv10822
Supporting Variants
SamplesNA19221
Known GenesC2, ZBTB12
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)nssv16710
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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