A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054824



Internal ID18797355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:124861873..124901623hg38UCSC Ensembl
Innerchr11:124731769..124771519hg19UCSC Ensembl
Innerchr11:124236979..124276729hg18UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3839751
hg1939751
hg1839751
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3516725
Samples
Known GenesROBO3, ROBO4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054824
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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