A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005929



Internal ID19095147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75383131..75527398hg38UCSC Ensembl
Innerchr3:75432282..75576549hg19UCSC Ensembl
Innerchr3:75514972..75659239hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38144268
hg19144268
hg18144268
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4776n100
Supporting Variantsnssv3596101
Samples
Known GenesFAM86DP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1005929
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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