A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011350



Internal ID19100567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75377944..75451601hg38UCSC Ensembl
Innerchr3:75427095..75500752hg19UCSC Ensembl
Innerchr3:75509785..75583442hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3873658
hg1973658
hg1873658
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4780n100
Supporting Variantsnssv3602009, nssv3602010
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)nsv1011350
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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