A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1003694



Internal ID16297650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:106134539..106138778hg38UCSC Ensembl
Innerchr4:107055696..107059935hg19UCSC Ensembl
Innerchr4:107275145..107279384hg18UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg384240
hg194240
hg184240
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv595009
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)nssv1003694
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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