A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044033



Internal ID19133252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:70168184..70205236hg38UCSC Ensembl
Innerchr13:70742316..70779368hg19UCSC Ensembl
Innerchr13:69640317..69677369hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3837053
hg1937053
hg1837053
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1712n100
Supporting Variantsnssv3529371
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)nsv1044033
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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