A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013155



Internal ID19102373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:62681587..62709238hg38UCSC Ensembl
Innerchr3:62667262..62694913hg19UCSC Ensembl
Innerchr3:62642302..62669953hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3827652
hg1927652
hg1827652
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4756n100
Supporting Variantsnssv3593443, nssv3593446, nssv3593441, nssv3593440, nssv3594556, nssv3593445, nssv3593442, nssv3593444, nssv3594554, nssv3594555, nssv3593439, nssv3594557
Samples
Known GenesCADPS
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013155
Frequency
Sample Size11257
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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