A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610150



Internal ID16397559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8240557..8287918hg38UCSC Ensembl
Innerchr8:8098079..8145440hg19UCSC Ensembl
Innerchr8:8135489..8182850hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3847362
hg1947362
hg1847362
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11937n54
Supporting Variantsnssv1156574, nssv1105881, nssv1105879, nssv1156571, nssv1156573, nssv1105878, nssv1105880, nssv1156572, nssv1156570, nssv1105877, nssv1105883, nssv1105882
Samples1780862274_A, NINDS_37, 1782681555_A, NINDS_152, 1782681176_A
Known GenesFAM86B3P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610150
Frequency
Sample Size17421
Observed Gain12
Observed Loss0
Observed Complex0
Frequencyn/a


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