A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3510541



Internal ID18462136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:49801903..50343061hg38UCSC Ensembl
Innerchr11:49823455..50302232hg19UCSC Ensembl
Innerchr11:49780031..50258808hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38541159
hg19478778
hg18478778
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048074
Supporting Variants
Samples
Known GenesLOC440040, LOC441601, OR4C12, OR4C13
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3510541
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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