A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050137



Internal ID19139356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:39516605..39544362hg38UCSC Ensembl
Innerchr13:40090742..40118499hg19UCSC Ensembl
Innerchr13:38988742..39016499hg18UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3827758
hg1927758
hg1827758
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3523389
Samples
Known GenesLHFP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050137
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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