A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045690



Internal ID18788221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:43055119..43096898hg38UCSC Ensembl
Innerchr10:43550567..43592346hg19UCSC Ensembl
Innerchr10:42870573..42912352hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3841780
hg1941780
hg1841780
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv723n100
Supporting Variantsnssv3507237, nssv3509305, nssv3517960
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)nsv1045690
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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