A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004609



Internal ID19093826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:137314568..137351321hg38UCSC Ensembl
Innerchr3:137033410..137070163hg19UCSC Ensembl
Innerchr3:138516100..138552853hg18UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3836754
hg1936754
hg1836754
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3608320
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)nsv1004609
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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