A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008271



Internal ID19097490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75383131..75496021hg38UCSC Ensembl
Innerchr3:75432282..75545172hg19UCSC Ensembl
Innerchr3:75514972..75627862hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38112891
hg19112891
hg18112891
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4774n100
Supporting Variantsnssv3733693, nssv3596096, nssv3596095, nssv3596097
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)nsv1008271
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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