A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3509649



Internal ID18461244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:43057447..43094310hg38UCSC Ensembl
Innerchr10:43552895..43589758hg19UCSC Ensembl
Innerchr10:42872901..42909764hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3836864
hg1936864
hg1836864
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039890
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)nssv3509649
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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