A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046203



Internal ID19135422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:9321914..9339414hg38UCSC Ensembl
Innerchr10:9363877..9381377hg19UCSC Ensembl
Innerchr10:9403883..9421383hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3817501
hg1917501
hg1817501
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3707684
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)nsv1046203
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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