A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14518



Internal ID15842720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32058417..32061134hg38UCSC Ensembl
Outerchr6:32057955..32061815hg38UCSC Ensembl
Innerchr6:32026194..32028911hg19UCSC Ensembl
Outerchr6:32025732..32029592hg19UCSC Ensembl
Innerchr6:32134172..32136889hg18UCSC Ensembl
Outerchr6:32133710..32137570hg18UCSC Ensembl
Innerchr6:32134172..32136889hg17UCSC Ensembl
Outerchr6:32133710..32137570hg17UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg383861
hg193861
hg183861
hg173861
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv10825
Supporting Variants
SamplesNA19144
Known GenesTNXB
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)nssv14518
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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