A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047813



Internal ID19137032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:42118976..42265456hg38UCSC Ensembl
Innerchr10:42614424..42760904hg19UCSC Ensembl
Innerchr10:41934430..42080910hg18UCSC Ensembl
Cytoband10q11.1
Allele length
AssemblyAllele length
hg38146481
hg19146481
hg18146481
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv716n100
Supporting Variantsnssv3707764, nssv3707765, nssv3707766
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)nsv1047813
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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