A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035449



Internal ID19124668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:19050964..19077346hg38UCSC Ensembl
Innerchr13:19625104..19651486hg19UCSC Ensembl
Innerchr13:18523104..18549486hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3826383
hg1926383
hg1826383
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3527561
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)nsv1035449
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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