A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595752



Internal ID16383161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:154314240..154412562hg38UCSC Ensembl
Innerchr4:155235392..155333714hg19UCSC Ensembl
Innerchr4:155454842..155553164hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3898323
hg1998323
hg1898323
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1009633
Samples
Known GenesDCHS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595752
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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