A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv946651



Internal ID16240607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:33931656..33982222hg38UCSC Ensembl
Innerchr21:35303960..35354523hg19UCSC Ensembl
Innerchr21:34225830..34276393hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3850567
hg1950564
hg1850564
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv587401
Supporting Variants
Samples
Known GenesLINC00649
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv946651
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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