A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009102



Internal ID18751633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:43243877..43328220hg38UCSC Ensembl
Innerchr3:43285369..43369712hg19UCSC Ensembl
Innerchr3:43260373..43344716hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3884344
hg1984344
hg1884344
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3589732
Samples
Known GenesSNRK
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009102
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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