A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043571



Internal ID19132790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:89808798..90276397hg38UCSC Ensembl
Innerchr10:91568555..92036154hg19UCSC Ensembl
Innerchr10:91558535..92026134hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38467600
hg19467600
hg18467600
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3706189
Samples
Known GenesLINC00865
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043571
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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