A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036146



Internal ID19125365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:15876551..15902138hg38UCSC Ensembl
Innerchr10:15918550..15944137hg19UCSC Ensembl
Innerchr10:15958556..15984143hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3825588
hg1925588
hg1825588
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3520317, nssv3522099
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)nsv1036146
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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