A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035764



Internal ID19124983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:90056944..90089561hg38UCSC Ensembl
Innerchr12:90450721..90483338hg19UCSC Ensembl
Innerchr12:88974852..89007469hg18UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg3832618
hg1932618
hg1832618
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1545n100
Supporting Variantsnssv3524812
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035764
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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