A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607537



Internal ID16048260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76035060..76048112hg38UCSC Ensembl
Innerchr7:75664378..75677430hg19UCSC Ensembl
Innerchr7:75502314..75515366hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3813053
hg1913053
hg1813053
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11459n54
Supporting Variantsnssv1087925
Samples
Known GenesMDH2, STYXL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607537
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