A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042522



Internal ID19131741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:52760817..52785442hg38UCSC Ensembl
Innerchr10:54520577..54545202hg19UCSC Ensembl
Innerchr10:54190583..54215208hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3824626
hg1924626
hg1824626
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv854n100
Supporting Variantsnssv3511186
Samples
Known GenesMBL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042522
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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