A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024591



Internal ID19113808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:18618452..18702307hg38UCSC Ensembl
Innerchr9:18618450..18702305hg19UCSC Ensembl
Innerchr9:18608450..18692305hg18UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3883856
hg1983856
hg1883856
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690676
Samples
Known GenesADAMTSL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024591
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