A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029572



Internal ID19118790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:25260928..25349470hg38UCSC Ensembl
Innerchr9:25260926..25349468hg19UCSC Ensembl
Innerchr9:25250926..25339468hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3888543
hg1988543
hg1888543
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7483n100
Supporting Variantsnssv3755864, nssv3690857
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)nsv1029572
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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