A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039505



Internal ID19128724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:4536019..4570057hg38UCSC Ensembl
Innerchr10:4578211..4612249hg19UCSC Ensembl
Innerchr10:4568211..4602249hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3834039
hg1934039
hg1834039
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3486356
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)nsv1039505
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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