A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012175



Internal ID19101393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:198762138..198808626hg38UCSC Ensembl
Innerchr1:198731267..198777755hg19UCSC Ensembl
Innerchr1:196997890..197044378hg18UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg3846489
hg1946489
hg1846489
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3492755
Samples
Known GenesMIR181A1HG
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012175
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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