A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035414



Internal ID19124633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:52759208..52776639hg38UCSC Ensembl
Innerchr10:54518968..54536399hg19UCSC Ensembl
Innerchr10:54188974..54206405hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3817432
hg1917432
hg1817432
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv855n100
Supporting Variantsnssv3503720
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)nsv1035414
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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