A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008563



Internal ID19097780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:138057309..138082552hg38UCSC Ensembl
Innerchr3:137776151..137801394hg19UCSC Ensembl
Innerchr3:139258841..139284084hg18UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3825244
hg1925244
hg1825244
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4907n100
Supporting Variantsnssv3741471, nssv3741470
Samples
Known GenesDZIP1L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1008563
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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