A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3523079



Internal ID18821360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:37813228..38514440hg38UCSC Ensembl
Innerchr12:38207030..38908242hg19UCSC Ensembl
Innerchr12:36493297..37194509hg18UCSC Ensembl
Cytoband12q11
Allele length
AssemblyAllele length
hg38701213
hg19701213
hg18701213
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047550
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)nssv3523079
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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