A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044855



Internal ID18787386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:109649225..109756261hg38UCSC Ensembl
Innerchr13:110301572..110408608hg19UCSC Ensembl
Innerchr13:109099573..109206609hg18UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38107037
hg19107037
hg18107037
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3713306
Samples
Known GenesIRS2, LINC00676
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044855
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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