A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595012



Internal ID16035735
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 StatusM
Merged Variantsdgv9194n54
Supporting Variantsnssv1003697, nssv1003699, nssv1003698
Samples
Known GenesTBCK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595012
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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