A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000430



Internal ID19089647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:145508846..145538536hg38UCSC Ensembl
Innerchr3:145226633..145256323hg19UCSC Ensembl
Innerchr3:146709323..146739013hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3829691
hg1929691
hg1829691
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4916n100
Supporting Variantsnssv3606139
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)nsv1000430
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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