A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042068



Internal ID19131287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32166460..32257538hg38UCSC Ensembl
Innerchr15:32458661..32549739hg19UCSC Ensembl
Innerchr15:30245953..30337031hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3891079
hg1991079
hg1891079
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2539n100
Supporting Variantsnssv3547723, nssv3547724, nssv3721609
Samples
Known GenesCHRNA7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042068
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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