A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006591



Internal ID19095808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:49032908..49063952hg38UCSC Ensembl
Innerchr4:49034925..49065969hg19UCSC Ensembl
Innerchr4:48729682..48760726hg18UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg3831045
hg1931045
hg1831045
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3625141, nssv3625140
Samples
Known GenesCWH43
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1006591
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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