A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv467643



Internal ID15527708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1616814..1629034hg38UCSC Ensembl
Innerchr11:1638044..1650264hg19UCSC Ensembl
Innerchr11:1594620..1606840hg18UCSC Ensembl
Innerchr11:1594620..1606840hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3812221
hg1912221
hg1812221
hg1712221
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv542863
SamplesHGDP00771
Known GenesKRTAP5-4, MOB2
MethodSNP array
AnalysisAn HMM examining LogR Ratio and B-allele Frequency was used to classify SNP array data into regions of copy-number 0-3. A combination of manual and automated curation was used on the resulting output to reduce false positives.
PlatformNot reported
Comments
ReferenceItsara_et_al_2009
Pubmed ID19166990
Accession Number(s)nsv467643
Frequency
Sample Size1557
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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