A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1295n100



Internal ID22787382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:127177506..127192623hg38UCSC Ensembl
chr11:127047401..127062518hg19UCSC Ensembl
chr11:126552611..126567728hg18UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3815118
hg1915118
hg1815118
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1044960, nsv1035192
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)dgv1295n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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