A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010264



Internal ID19099482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75383131..75511978hg38UCSC Ensembl
Innerchr3:75432282..75561129hg19UCSC Ensembl
Innerchr3:75514972..75643819hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38128848
hg19128848
hg18128848
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4776n100
Supporting Variantsnssv3596100, nssv3596099
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)nsv1010264
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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