A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv813154



Internal ID16107110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:65952487..66019751hg38UCSC Ensembl
Innerchr13:66526619..66593883hg19UCSC Ensembl
Innerchr13:65424620..65491884hg18UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3867265
hg1967265
hg1867265
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562095
Supporting Variants
Samples
Known GenesMIR548X2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv813154
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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