A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615427



Internal ID16402836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:129384126..129405288hg38UCSC Ensembl
Innerchr9:132146405..132167567hg19UCSC Ensembl
Innerchr9:131186226..131207388hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3821163
hg1921163
hg1821163
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12892n54
Supporting Variantsnssv1176151, nssv1176150, nssv1176152
SamplesNINDS_60, NINDS_98, NINDS_59
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615427
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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