A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595044



Internal ID16382453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:106138778..106141514hg38UCSC Ensembl
Innerchr4:107059935..107062671hg19UCSC Ensembl
Innerchr4:107279384..107282120hg18UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg382737
hg192737
hg182737
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9200n54
Supporting Variantsnssv1003968, nssv1003967
Samples
Known GenesTBCK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595044
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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