A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011406



Internal ID19100623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:34625148..34638878hg38UCSC Ensembl
Innerchr1:35090749..35104479hg19UCSC Ensembl
Innerchr1:34863336..34877066hg18UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3813731
hg1913731
hg1813731
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv146n100
Supporting Variantsnssv3700638, nssv3700640, nssv3479319, nssv3475655, nssv3700639, nssv3473025, nssv3477421, nssv3476950, nssv3478368, nssv3482017, nssv3480225, nssv3467596, nssv3467468, nssv3470328, nssv3463688, nssv3463152, nssv3470200, nssv3466871, nssv3475177, nssv3471320, nssv3464601, nssv3479488, nssv3466269, nssv3468815
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)nsv1011406
Frequency
Sample Size11257
Observed Gain0
Observed Loss24
Observed Complex0
Frequencyn/a


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