A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004324



Internal ID19093541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:164111551..164201121hg38UCSC Ensembl
Innerchr3:163829339..163918909hg19UCSC Ensembl
Innerchr3:165312033..165401603hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3889571
hg1989571
hg1889571
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3614536
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)nsv1004324
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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