A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3522728



Internal ID18474323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:43057447..43096169hg38UCSC Ensembl
Innerchr10:43552895..43591617hg19UCSC Ensembl
Innerchr10:42872901..42911623hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3838723
hg1938723
hg1838723
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046759
Supporting Variants
Samples
Known GenesRET
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3522728
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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