A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3625024



Internal ID18923305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:35675889..35715858hg38UCSC Ensembl
Innerchr4:35677511..35717480hg19UCSC Ensembl
Innerchr4:35353906..35393875hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3839970
hg1939970
hg1839970
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1013874
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)nssv3625024
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