A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1257n100



Internal ID22787344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:97086703..97176950hg38UCSC Ensembl
chr11:96957703..97047950hg19UCSC Ensembl
chr11:96462913..96553160hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3890248
hg1990248
hg1890248
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1038441, nsv1037706, nsv1043735, nsv1040083, nsv1050484, nsv1035786, nsv1053050, nsv1041811
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)dgv1257n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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