A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524054



Internal ID15451347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:86172914..86212377hg38UCSC Ensembl
Innerchr7:85802230..85841693hg19UCSC Ensembl
Innerchr7:85640166..85679629hg18UCSC Ensembl
Innerchr7:85446881..85486344hg17UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3839464
hg1939464
hg1839464
hg1739464
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699920
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524054
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