A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3711833



Internal ID18663428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:65487421..66772963hg38UCSC Ensembl
Innerchr13:66061553..67347095hg19UCSC Ensembl
Innerchr13:64959554..66245096hg18UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg381285543
hg191285543
hg181285543
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043603
Supporting Variants
Samples
Known GenesMIR4704, MIR548X2, PCDH9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3711833
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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