A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153377



Internal ID15881291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:180749005..180799673hg38UCSC Ensembl
Innerchr5:180176005..180226673hg19UCSC Ensembl
Innerchr5:180108611..180159279hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3850669
hg1950669
hg1850669
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv600678
Supporting Variants
SamplesNINDS_96
Known GenesMGAT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153377
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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