A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012061



Internal ID19101279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:412575..445782hg38UCSC Ensembl
Innerchr4:406364..439571hg19UCSC Ensembl
Innerchr4:396364..429571hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3833208
hg1933208
hg1833208
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3616093, nssv3616094, nssv3616095, nssv3616097, nssv3616096
Samples
Known GenesABCA11P, ZNF721
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012061
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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