A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035192



Internal ID19124411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:127178395..127192623hg38UCSC Ensembl
Innerchr11:127048290..127062518hg19UCSC Ensembl
Innerchr11:126553500..126567728hg18UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3814229
hg1914229
hg1814229
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1295n100
Supporting Variantsnssv3710765
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)nsv1035192
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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