A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000158



Internal ID19089375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:61612888..61697214hg38UCSC Ensembl
Innerchr3:61598562..61682888hg19UCSC Ensembl
Innerchr3:61573602..61657928hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3884327
hg1984327
hg1884327
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4755n100
Supporting Variantsnssv3593435
Samples
Known GenesPTPRG
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1000158
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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