A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3710053



Internal ID19008334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:19588241..19619267hg38UCSC Ensembl
Innerchr11:19609788..19640813hg19UCSC Ensembl
Innerchr11:19566364..19597389hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3831027
hg1931026
hg1831026
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048120
Supporting Variants
Samples
Known GenesNAV2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3710053
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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