A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953321



Internal ID17302195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:8986668..9093367hg38UCSC Ensembl
Outerchr21:9825501..9932200hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg38106700
hg19106700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000031
SamplesBILGI_BIOE
Known GenesMIR3648, MIR3687, TEKT4P2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953321
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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