A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041937



Internal ID19131156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:90046848..90099921hg38UCSC Ensembl
Innerchr12:90440625..90493698hg19UCSC Ensembl
Innerchr12:88964756..89017829hg18UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg3853074
hg1953074
hg1853074
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1544n100
Supporting Variantsnssv3524808, nssv3524809
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)nsv1041937
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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