A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036471



Internal ID19125690
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 StatusM
Merged Variantsdgv1485n100
Supporting Variantsnssv3523083
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)nsv1036471
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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