A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041014



Internal ID19130233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5761683..5791118hg38UCSC Ensembl
Innerchr11:5782913..5812348hg19UCSC Ensembl
Innerchr11:5739489..5768924hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3829436
hg1929436
hg1829436
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1044n100
Supporting Variantsnssv3508957, nssv3521110, nssv3707255, nssv3504866, nssv3503667
Samples
Known GenesOR52N1, OR52N5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041014
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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