A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041915



Internal ID19131134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:95091691..95109937hg38UCSC Ensembl
Innerchr10:96851448..96869694hg19UCSC Ensembl
Innerchr10:96841438..96859684hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3818247
hg1918247
hg1818247
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3510603, nssv3507264, nssv3706201, nssv3518738, nssv3706200
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)nsv1041915
Frequency
Sample Size11257
Observed Gain4
Observed Loss1
Observed Complex0
Frequencyn/a


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