A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008745



Internal ID19097962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:105805675..105909559hg38UCSC Ensembl
Innerchr1:106348297..106452181hg19UCSC Ensembl
Innerchr1:106149820..106253704hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38103885
hg19103885
hg18103885
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3502198
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)nsv1008745
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