A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3625136



Internal ID18923417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:48171930..48184627hg38UCSC Ensembl
Innerchr4:48173947..48186644hg19UCSC Ensembl
Innerchr4:47868704..47881401hg18UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3812698
hg1912698
hg1812698
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1011366
Supporting Variants
Samples
Known GenesTEC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3625136
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