A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019825



Internal ID19109043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64480573..64809880hg38UCSC Ensembl
Innerchr9:69492991..69822298hg19UCSC Ensembl
Innerchr9:68782811..69112118hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38329308
hg19329308
hg18329308
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7655n100
Supporting Variantsnssv3696139
Samples
Known GenesLOC100133920
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019825
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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