A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169649



Internal ID21313460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:112839104..112882313hg38UCSC Ensembl
Outerchr13:112835851..112888145hg38UCSC Ensembl
Innerchr13:113493418..113536627hg19UCSC Ensembl
Outerchr13:113490165..113542459hg19UCSC Ensembl
Innerchr13:112541419..112584628hg18UCSC Ensembl
Outerchr13:112538166..112590460hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3852295
hg1952295
hg1852295
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14247392
SamplesNGO_25
Known GenesATP11A
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169649
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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