A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000897



Internal ID19090114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:218870392..218933864hg38UCSC Ensembl
Innerchr1:219043734..219107206hg19UCSC Ensembl
Innerchr1:217110357..217173829hg18UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3863473
hg1963473
hg1863473
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3705517
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)nsv1000897
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