A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028793



Internal ID19118011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:28588577..28768828hg38UCSC Ensembl
Innerchr9:28588575..28768826hg19UCSC Ensembl
Innerchr9:28578575..28758826hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38180252
hg19180252
hg18180252
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7491n100
Supporting Variantsnssv3755890
Samples
Known GenesLINGO2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028793
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