A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1255n100



Internal ID22787342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:96447445..96550811hg38UCSC Ensembl
chr11:96180609..96283976hg19UCSC Ensembl
chr11:95820257..95923624hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38103367
hg19103368
hg18103368
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1044697, nsv1036329, nsv1042360, nsv1035691, nsv1050531
Samples
Known GenesJRKL-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1255n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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