A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999213



Internal ID19158749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75377944..75478042hg38UCSC Ensembl
Innerchr3:75427095..75527193hg19UCSC Ensembl
Innerchr3:75509785..75609883hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38100099
hg19100099
hg18100099
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4774n100
Supporting Variantsnssv3602031, nssv3733048
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)nsv999213
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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