A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046110



Internal ID19135329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:130544488..130601384hg38UCSC Ensembl
Innerchr10:132342752..132399648hg19UCSC Ensembl
Innerchr10:132232742..132289638hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3856897
hg1956897
hg1856897
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3517772
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)nsv1046110
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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