A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006892



Internal ID19096110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:208265627..208283580hg38UCSC Ensembl
Innerchr1:208438972..208456925hg19UCSC Ensembl
Innerchr1:206505595..206523548hg18UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3817954
hg1917954
hg1817954
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv566n100
Supporting Variantsnssv3500971, nssv3500191, nssv3492732, nssv3484998, nssv3499220, nssv3493415, nssv3482849, nssv3489964, nssv3486600, nssv3486653, nssv3501725, nssv3490956, nssv3495190
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)nsv1006892
Frequency
Sample Size11257
Observed Gain13
Observed Loss0
Observed Complex0
Frequencyn/a


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