A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3503989



Internal ID18802270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:50135065..50614043hg38UCSC Ensembl
Innerchr11:50094236..50573214hg19UCSC Ensembl
Innerchr11:50050812..50529790hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38478979
hg19478979
hg18478979
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035641
Supporting Variants
Samples
Known GenesLOC441601, LOC646813
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3503989
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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