A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3523083



Internal ID18821364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:37885529..38449639hg38UCSC Ensembl
Innerchr12:38279331..38843441hg19UCSC Ensembl
Innerchr12:36565598..37129708hg18UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg38564111
hg19564111
hg18564111
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036471
Supporting Variants
Samples
Known GenesALG10B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3523083
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