A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174950



Internal ID15527938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:102465886..102543212hg38UCSC Ensembl
Innerchr11:102336617..102413943hg19UCSC Ensembl
Innerchr11:101841827..101919153hg18UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg3877327
hg1977327
hg1877327
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556151
Supporting Variants
SamplesHGDP00563
Known GenesMMP7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174950
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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