A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057872



Internal ID19147091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10524034..10582038hg38UCSC Ensembl
Innerchr21:10930419..10988423hg19UCSC Ensembl
Innerchr21:9952290..10010294hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg3858005
hg1958005
hg1858005
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4361n100
Supporting Variantsnssv3732536
Samples
Known GenesTPTE
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057872
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