A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1097n100



Internal ID22787184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:37319835..37363266hg38UCSC Ensembl
chr11:37341385..37384816hg19UCSC Ensembl
chr11:37297961..37341392hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3843432
hg1943432
hg1843432
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1044627, nsv1050145, nsv1042230
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)dgv1097n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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