A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv963382



Internal ID16257338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:59774392..59841052hg38UCSC Ensembl
Innerchr3:59760118..59826778hg19UCSC Ensembl
Innerchr3:59735158..59801818hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3866661
hg1966661
hg1866661
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590381
Supporting Variants
Samples
Known GenesFHIT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv963382
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