A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049061



Internal ID19138280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:81561781..82120651hg38UCSC Ensembl
Innerchr13:82135916..82694786hg19UCSC Ensembl
Innerchr13:81033917..81592787hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38558871
hg19558871
hg18558871
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1716n100
Supporting Variantsnssv3530533, nssv3530534
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049061
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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