A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv753954



Internal ID16047910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:91908353..91908906hg38UCSC Ensembl
Innerchr10:93668110..93668663hg19UCSC Ensembl
Innerchr10:93658090..93658643hg18UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg38554
hg19554
hg18554
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551921
Supporting Variants
Samples
Known GenesFGFBP3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv753954
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