A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010072



Internal ID19099291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75366712..75499571hg38UCSC Ensembl
Innerchr3:75415863..75548722hg19UCSC Ensembl
Innerchr3:75498553..75631412hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38132860
hg19132860
hg18132860
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4774n100
Supporting Variantsnssv3732985
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)nsv1010072
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer