A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042211



Internal ID19131430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:75959088..75987347hg38UCSC Ensembl
Innerchr13:76533224..76561483hg19UCSC Ensembl
Innerchr13:75431225..75459484hg18UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg3828260
hg1928260
hg1828260
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3713240
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042211
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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