A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059744



Internal ID18802275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:33647795..33688348hg38UCSC Ensembl
Innerchr21:35020101..35060653hg19UCSC Ensembl
Innerchr21:33941971..33982523hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3840554
hg1940553
hg1840553
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3600131
Samples
Known GenesITSN1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059744
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer