A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004088



Internal ID19093305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75372007..75511978hg38UCSC Ensembl
Innerchr3:75421158..75561129hg19UCSC Ensembl
Innerchr3:75503848..75643819hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38139972
hg19139972
hg18139972
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4776n100
Supporting Variantsnssv3733000, nssv3594981, nssv3594982, nssv3594984, nssv3594983
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)nsv1004088
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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