A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045672



Internal ID19134891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:107369429..107396152hg38UCSC Ensembl
Innerchr10:109129187..109155910hg19UCSC Ensembl
Innerchr10:109119177..109145900hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3826724
hg1926724
hg1826724
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv971n100
Supporting Variantsnssv3515445
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)nsv1045672
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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