A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3646994



Internal ID18945275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:108034378..108099613hg38UCSC Ensembl
Innerchr5:107370079..107435314hg19UCSC Ensembl
Innerchr5:107397978..107463213hg18UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3865236
hg1965236
hg1865236
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029650
Supporting Variants
Samples
Known GenesFBXL17
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3646994
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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