A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035755



Internal ID19124974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:30906647..31242391hg38UCSC Ensembl
Innerchr11:30928194..31263938hg19UCSC Ensembl
Innerchr11:30884770..31220514hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38335745
hg19335745
hg18335745
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3504106
Samples
Known GenesDCDC5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035755
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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