A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011871



Internal ID18754406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:143673260..143735180hg38UCSC Ensembl
Innerchr1:149167900..149229831hg19UCSC Ensembl
Innerchr1:147434524..147496455hg18UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg3861921
hg1961932
hg1861932
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3704206
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)nsv1011871
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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