A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595656



Internal ID16383065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:148177785..148179361hg38UCSC Ensembl
Innerchr4:149098936..149100512hg19UCSC Ensembl
Innerchr4:149318386..149319962hg18UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg381577
hg191577
hg181577
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9307n54
Supporting Variantsnssv1009333
Samples
Known GenesNR3C2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595656
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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