A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703122



Internal ID15439774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:141127393..141140792hg38UCSC Ensembl
Innerchr4:142048547..142061946hg19UCSC Ensembl
Innerchr4:142267997..142281396hg18UCSC Ensembl
Innerchr4:142406152..142419551hg17UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3813400
hg1913400
hg1813400
hg1713400
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526770
Supporting Variants
Samples
Known GenesRNF150
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703122
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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