A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043548



Internal ID19132767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:105324556..105374322hg38UCSC Ensembl
Innerchr10:107084314..107134080hg19UCSC Ensembl
Innerchr10:107074304..107124070hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3849767
hg1949767
hg1849767
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3706214
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)nsv1043548
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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