A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595657



Internal ID16383066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:148177785..148179570hg38UCSC Ensembl
Innerchr4:149098936..149100721hg19UCSC Ensembl
Innerchr4:149318386..149320171hg18UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg381786
hg191786
hg181786
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9307n54
Supporting Variantsnssv1009334
Samples
Known GenesNR3C2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595657
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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