A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032967



Internal ID19122189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7985651..8088281hg38UCSC Ensembl
Innerchr9:7985651..8088281hg19UCSC Ensembl
Innerchr9:7975651..8078281hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38102631
hg19102631
hg18102631
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7394n100
Supporting Variantsnssv3758118
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)nsv1032967
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