A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052089



Internal ID18794620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:24009607..24031661hg38UCSC Ensembl
Innerchr13:24583746..24605800hg19UCSC Ensembl
Innerchr13:23481746..23503800hg18UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg3822055
hg1922055
hg1822055
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3523158
Samples
Known GenesSPATA13
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052089
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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