A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974243



Internal ID18609455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:92913933..92923007hg38UCSC Ensembl
Innerchr13:93566186..93575260hg19UCSC Ensembl
Innerchr13:92364187..92373261hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg389075
hg199075
hg189075
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2759279
SamplesHGDP00998
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv974243
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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