A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv677268



Internal ID15413920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:50230418..50255260hg38UCSC Ensembl
Innerchr7:50270014..50294856hg19UCSC Ensembl
Innerchr7:50240560..50265402hg18UCSC Ensembl
Innerchr7:50047275..50072117hg17UCSC Ensembl
Cytoband7p12.2
Allele length
AssemblyAllele length
hg3824843
hg1924843
hg1824843
hg1724843
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520090
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv677268
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