A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002352



Internal ID19091569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75372007..75493683hg38UCSC Ensembl
Innerchr3:75421158..75542834hg19UCSC Ensembl
Innerchr3:75503848..75625524hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38121677
hg19121677
hg18121677
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4774n100
Supporting Variantsnssv3732989, nssv3594967, nssv3594968
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)nsv1002352
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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