A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035857



Internal ID18778388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:21319810..21346637hg38UCSC Ensembl
Innerchr13:21893949..21920776hg19UCSC Ensembl
Innerchr13:20791949..20818776hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3826828
hg1926828
hg1826828
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1613n100
Supporting Variantsnssv3523135
Samples
Known GenesLINC00539, MIPEPP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035857
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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