A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002800



Internal ID19092017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:24883232..24901114hg38UCSC Ensembl
Innerchr3:24924723..24942605hg19UCSC Ensembl
Innerchr3:24899727..24917609hg18UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3817883
hg1917883
hg1817883
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4703n100
Supporting Variantsnssv3589505
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)nsv1002800
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