A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002182



Internal ID19091399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:164549841..164589658hg38UCSC Ensembl
Innerchr3:164267629..164307446hg19UCSC Ensembl
Innerchr3:165750323..165790140hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3839818
hg1939818
hg1839818
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3614544
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)nsv1002182
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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