A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606478



Internal ID16393887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:28534799..28535336hg38UCSC Ensembl
Innerchr7:28574417..28574954hg19UCSC Ensembl
Innerchr7:28540942..28541479hg18UCSC Ensembl
Cytoband7p15.1
Allele length
AssemblyAllele length
hg38538
hg19538
hg18538
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11247n54
Supporting Variantsnssv1081710, nssv1081707, nssv1081706, nssv1081708, nssv1081713, nssv1081712, nssv1081709, nssv1081711
Samples
Known GenesCREB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606478
Frequency
Sample Size17421
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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