A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033156



Internal ID19122378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39455352..39747836hg38UCSC Ensembl
Innerchr9:41600370..41892854hg19UCSC Ensembl
Innerchr9:41590370..41882854hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38292485
hg19292485
hg18292485
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7546n100
Supporting Variantsnssv3755948
Samples
Known GenesLOC653501
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033156
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