A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006451



Internal ID19095668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:137419399..137535542hg38UCSC Ensembl
Innerchr3:137138241..137254384hg19UCSC Ensembl
Innerchr3:138620931..138737074hg18UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg38116144
hg19116144
hg18116144
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4905n100
Supporting Variantsnssv3608321
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)nsv1006451
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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