A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050001



Internal ID19139220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55676723..55836092hg38UCSC Ensembl
Innerchr11:55444199..55603568hg19UCSC Ensembl
Innerchr11:55200775..55360144hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38159370
hg19159370
hg18159370
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1204n100
Supporting Variantsnssv3509841, nssv3507587
Samples
Known GenesOR5D13, OR5D14, OR5D18, OR5L1, OR5L2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050001
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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