A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040642



Internal ID18783173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46395843..46437212hg38UCSC Ensembl
Innerchr10:47112547..47153919hg19UCSC Ensembl
Innerchr10:46532553..46573925hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3841370
hg1941373
hg1841373
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv822n100
Supporting Variantsnssv3507845
Samples
Known GenesHNRNPA1P33, LINC00842
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040642
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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