A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035850



Internal ID19125069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:37813228..38518710hg38UCSC Ensembl
Innerchr12:38207030..38912512hg19UCSC Ensembl
Innerchr12:36493297..37198779hg18UCSC Ensembl
Cytoband12q11
Allele length
AssemblyAllele length
hg38705483
hg19705483
hg18705483
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1485n100
Supporting Variantsnssv3523080
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)nsv1035850
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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