A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007785



Internal ID19097004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75372007..75483268hg38UCSC Ensembl
Innerchr3:75421158..75532419hg19UCSC Ensembl
Innerchr3:75503848..75615109hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38111262
hg19111262
hg18111262
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4774n100
Supporting Variantsnssv3594965
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)nsv1007785
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