A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022168



Internal ID18764702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:111074268..111122810hg38UCSC Ensembl
Innerchr5:110409966..110458508hg19UCSC Ensembl
Innerchr5:110437865..110486407hg18UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg3848543
hg1948543
hg1848543
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5780n100
Supporting Variantsnssv3746561
Samples
Known GenesTSLP, WDR36
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022168
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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