A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3591628



Internal ID18543223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4195352..4237761hg38UCSC Ensembl
Innerchr3:4237036..4279445hg19UCSC Ensembl
Innerchr3:4212036..4254445hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3842410
hg1942410
hg1842410
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1007191
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3591628
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