A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3527549



Internal ID18825830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18471488..18892419hg38UCSC Ensembl
Innerchr13:19045628..19466559hg19UCSC Ensembl
Innerchr13:17943628..18364559hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg38420932
hg19420932
hg18420932
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051306
Supporting Variants
Samples
Known GenesANKRD20A9P, LINC00417
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3527549
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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