A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043516



Internal ID18786047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:103980929..104009998hg38UCSC Ensembl
Innerchr10:105740687..105769756hg19UCSC Ensembl
Innerchr10:105730677..105759746hg18UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg3829070
hg1929070
hg1829070
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv967n100
Supporting Variantsnssv3510030
Samples
Known GenesSLK
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043516
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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