A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019151



Internal ID19108369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136669376..136849436hg38UCSC Ensembl
Innerchr8:137681619..137861679hg19UCSC Ensembl
Innerchr8:137750801..137930861hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38180061
hg19180061
hg18180061
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7325n100
Supporting Variantsnssv3757391, nssv3757390, nssv3757389
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)nsv1019151
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer