A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614329



Internal ID16401738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39445501..39588135hg38UCSC Ensembl
Innerchr9:41586495..41733153hg19UCSC Ensembl
Innerchr9:41576495..41723153hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38142635
hg19146659
hg18146659
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1134181
Samples
Known GenesLOC653501, ZNF658B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614329
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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