A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1003968



Internal ID16297924
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 StatusS
Merged Variantsnsv595044
Supporting Variants
Samples
Known GenesTBCK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1003968
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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