A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605689



Internal ID16046412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:551684..552205hg38UCSC Ensembl
Innerchr7:591321..591842hg19UCSC Ensembl
Innerchr7:557847..558368hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38522
hg19522
hg18522
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11108n54
Supporting Variantsnssv1077798
Samples
Known GenesPRKAR1B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605689
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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