A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17315



Internal ID15829063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:47471874..47471987hg38UCSC Ensembl
Outerchr10:47471474..47472324hg38UCSC Ensembl
Innerchr10:48267375..48267488hg19UCSC Ensembl
Outerchr10:48267038..48267888hg19UCSC Ensembl
Innerchr10:47887381..47887494hg18UCSC Ensembl
Outerchr10:47887044..47887894hg18UCSC Ensembl
Innerchr10:47887381..47887494hg17UCSC Ensembl
Outerchr10:47887044..47887894hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38851
hg19851
hg18851
hg17851
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8636
Supporting Variants
SamplesNA10847
Known GenesANXA8
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)nssv17315
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer