A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv678870



Internal ID15415522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:15100292..15104412hg38UCSC Ensembl
Innerchr4:15101916..15106036hg19UCSC Ensembl
Innerchr4:14711014..14715134hg18UCSC Ensembl
Innerchr4:14778185..14782305hg17UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg384121
hg194121
hg184121
hg174121
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517324
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv678870
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