A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043842



Internal ID19133061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:97380089..97602215hg38UCSC Ensembl
Innerchr11:97251089..97473215hg19UCSC Ensembl
Innerchr11:96756299..96978425hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38222127
hg19222127
hg18222127
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3710717
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)nsv1043842
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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