A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595584



Internal ID16036307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:139307654..139317207hg38UCSC Ensembl
Innerchr4:140228808..140238361hg19UCSC Ensembl
Innerchr4:140448258..140457811hg18UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg389554
hg199554
hg189554
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9292n54
Supporting Variantsnssv1008212, nssv1008213
Samples
Known GenesNAA15
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595584
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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