A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv807722



Internal ID16101678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:35573528..35682080hg38UCSC Ensembl
Innerchr13:36147665..36256217hg19UCSC Ensembl
Innerchr13:35045665..35154217hg18UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38108553
hg19108553
hg18108553
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv561483
Supporting Variants
Samples
Known GenesMIR548F5, NBEA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv807722
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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