A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042082



Internal ID19131301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:88165284..88204393hg38UCSC Ensembl
Innerchr11:87898452..87937561hg19UCSC Ensembl
Innerchr11:87538100..87577209hg18UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3839110
hg1939110
hg1839110
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3508975
Samples
Known GenesRAB38
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042082
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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