A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3639363



Internal ID18590958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:121352476..121370988hg38UCSC Ensembl
Innerchr4:122273631..122292143hg19UCSC Ensembl
Innerchr4:122493081..122511593hg18UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3818513
hg1918513
hg1818513
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1014710
Supporting Variants
Samples
Known GenesQRFPR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3639363
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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