A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044185



Internal ID19133404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:87297480..87444389hg38UCSC Ensembl
Innerchr13:87949735..88096644hg19UCSC Ensembl
Innerchr13:86747736..86894645hg18UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg38146910
hg19146910
hg18146910
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525445
Samples
Known GenesMIR4500HG
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044185
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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