A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3733907



Internal ID19032188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75377944..75571732hg38UCSC Ensembl
Innerchr3:75427095..75620883hg19UCSC Ensembl
Innerchr3:75509785..75703573hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38193789
hg19193789
hg18193789
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1009577
Supporting Variants
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)nssv3733907
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