A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3525517



Internal ID18823798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:97223320..97302880hg38UCSC Ensembl
Innerchr13:97875574..97955134hg19UCSC Ensembl
Innerchr13:96673575..96753135hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3879561
hg1979561
hg1879561
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1045777
Supporting Variants
Samples
Known GenesMBNL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3525517
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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