A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050698



Internal ID19139917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:83998215..84017502hg38UCSC Ensembl
Innerchr10:85757971..85777258hg19UCSC Ensembl
Innerchr10:85747951..85767238hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3819288
hg1919288
hg1819288
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv946n100
Supporting Variantsnssv3506132, nssv3520737
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)nsv1050698
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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