A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025551



Internal ID19114769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:117409429..117420332hg38UCSC Ensembl
Innerchr6:117730592..117741495hg19UCSC Ensembl
Innerchr6:117837285..117848188hg18UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg3810904
hg1910904
hg1810904
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6141n100
Supporting Variantsnssv3654324, nssv3749517, nssv3654327, nssv3654323, nssv3749518, nssv3654326, nssv3654325, nssv3654321, nssv3654322
Samples
Known GenesROS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025551
Frequency
Sample Size11257
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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