A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1003699



Internal ID15950969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:106134539..106141514hg38UCSC Ensembl
Innerchr4:107055696..107062671hg19UCSC Ensembl
Innerchr4:107275145..107282120hg18UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg386976
hg196976
hg186976
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv595012
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)nssv1003699
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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