A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052508



Internal ID19141727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:130547233..130772530hg38UCSC Ensembl
Innerchr10:132345497..132570794hg19UCSC Ensembl
Innerchr10:132235487..132460784hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38225298
hg19225298
hg18225298
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3514965
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)nsv1052508
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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