A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041130



Internal ID19130349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:95105415..95122745hg38UCSC Ensembl
Innerchr10:96865172..96882502hg19UCSC Ensembl
Innerchr10:96855162..96872492hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3817331
hg1917331
hg1817331
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv962n100
Supporting Variantsnssv3510895
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)nsv1041130
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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