A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010254



Internal ID19099472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:176175294..176231852hg38UCSC Ensembl
Innerchr3:175893082..175949640hg19UCSC Ensembl
Innerchr3:177375776..177432334hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3856559
hg1956559
hg1856559
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4992n100
Supporting Variantsnssv3614931
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)nsv1010254
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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