A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169577



Internal ID21313810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:64415638..64468699hg38UCSC Ensembl
Outerchr13:64409207..64475252hg38UCSC Ensembl
Innerchr13:64989770..65042831hg19UCSC Ensembl
Outerchr13:64983339..65049384hg19UCSC Ensembl
Innerchr13:63887771..63940832hg18UCSC Ensembl
Outerchr13:63881340..63947385hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3866046
hg1966046
hg1866046
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14251040
SamplesSNI_14
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169577
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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