A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018195



Internal ID19107412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:5682419..5715007hg38UCSC Ensembl
Innerchr5:5682532..5715120hg19UCSC Ensembl
Innerchr5:5735532..5768120hg18UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg3832589
hg1932589
hg1832589
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5555n100
Supporting Variantsnssv3746175, nssv3638575, nssv3638585, nssv3638577, nssv3638584, nssv3638581, nssv3746177, nssv3638574, nssv3638582, nssv3638586, nssv3746176, nssv3638579, nssv3638576, nssv3638580, nssv3638583, nssv3746178, nssv3638573, nssv3638578
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018195
Frequency
Sample Size11257
Observed Gain18
Observed Loss0
Observed Complex0
Frequencyn/a


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