A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608440



Internal ID16395849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:133389726..133438540hg38UCSC Ensembl
Innerchr7:133074480..133123294hg19UCSC Ensembl
Innerchr7:132725020..132773834hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3848815
hg1948815
hg1848815
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1094544
Samples
Known GenesEXOC4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608440
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