A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705156



Internal ID15441808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:9018053..9196395hg38UCSC Ensembl
Innerchr7:9057683..9236025hg19UCSC Ensembl
Innerchr7:9024208..9202550hg18UCSC Ensembl
Innerchr7:8830923..9009265hg17UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38178343
hg19178343
hg18178343
hg17178343
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528544
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705156
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