A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595734



Internal ID16383143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:152014403..152071589hg38UCSC Ensembl
Innerchr4:152935555..152992741hg19UCSC Ensembl
Innerchr4:153155005..153212191hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3857187
hg1957187
hg1857187
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1009600
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595734
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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