A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050571



Internal ID19139790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:11395684..11424750hg38UCSC Ensembl
Innerchr10:11437683..11466749hg19UCSC Ensembl
Innerchr10:11477689..11506755hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3829067
hg1929067
hg1829067
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv672n100
Supporting Variantsnssv3494579
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)nsv1050571
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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