A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3506034



Internal ID18457629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:9433840..9514423hg38UCSC Ensembl
Innerchr11:9455387..9535970hg19UCSC Ensembl
Innerchr11:9411963..9492546hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3880584
hg1980584
hg1880584
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039537
Supporting Variants
Samples
Known GenesIPO7, LOC644656, ZNF143
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3506034
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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