A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032258



Internal ID19121480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:25260928..25353889hg38UCSC Ensembl
Innerchr9:25260926..25353887hg19UCSC Ensembl
Innerchr9:25250926..25343887hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3892962
hg1992962
hg1892962
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7483n100
Supporting Variantsnssv3691983
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)nsv1032258
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