A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1003695



Internal ID16297651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:106134539..106139684hg38UCSC Ensembl
Innerchr4:107055696..107060841hg19UCSC Ensembl
Innerchr4:107275145..107280290hg18UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg385146
hg195146
hg185146
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv595010
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)nssv1003695
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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