A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043751



Internal ID19132970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:80616973..80657274hg38UCSC Ensembl
Innerchr13:81191108..81231409hg19UCSC Ensembl
Innerchr13:80089109..80129410hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3840302
hg1940302
hg1840302
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3530528
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)nsv1043751
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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