A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3636851



Internal ID18588446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:32106978..32155435hg38UCSC Ensembl
Innerchr5:32107084..32155541hg19UCSC Ensembl
Innerchr5:32142841..32191298hg18UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3848458
hg1948458
hg1848458
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030952
Supporting Variants
Samples
Known GenesGOLPH3, PDZD2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3636851
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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