A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3630969



Internal ID18929250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:92634401..92716216hg38UCSC Ensembl
Innerchr4:93555552..93637367hg19UCSC Ensembl
Innerchr4:93774575..93856390hg18UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3881816
hg1981816
hg1881816
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1014347
Supporting Variants
Samples
Known GenesGRID2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3630969
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