A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012322



Internal ID18754855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:97894388..97985590hg38UCSC Ensembl
Innerchr3:97613232..97704434hg19UCSC Ensembl
Innerchr3:99095922..99187124hg18UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3891203
hg1991203
hg1891203
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3603320
Samples
Known GenesCRYBG3, MINA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012322
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