A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608980



Internal ID16049703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:149748496..149786285hg38UCSC Ensembl
Innerchr7:149445585..149483373hg19UCSC Ensembl
Innerchr7:149076518..149114306hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3837790
hg1937789
hg1837789
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11714n54
Supporting Variantsnssv1099472
Samples
Known GenesSSPO, ZNF467
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608980
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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