A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018096



Internal ID19107313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:103279597..103314174hg38UCSC Ensembl
Innerchr6:103727472..103762049hg19UCSC Ensembl
Innerchr6:103834165..103868742hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3834578
hg1934578
hg1834578
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6119n100
Supporting Variantsnssv3649925, nssv3649935, nssv3649932, nssv3649939, nssv3649919, nssv3649922, nssv3649942, nssv3649920, nssv3649940, nssv3649934, nssv3649927, nssv3649930, nssv3649921, nssv3649926, nssv3649924, nssv3649941, nssv3649938, nssv3649929, nssv3649923, nssv3649933, nssv3649931, nssv3649936, nssv3649937, nssv3649928
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)nsv1018096
Frequency
Sample Size11257
Observed Gain11
Observed Loss13
Observed Complex0
Frequencyn/a


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