A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035909



Internal ID18778440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:58191397..58251260hg38UCSC Ensembl
Innerchr13:58765531..58825394hg19UCSC Ensembl
Innerchr13:57663532..57723395hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3859864
hg1959864
hg1859864
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3711765
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)nsv1035909
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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