A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1009756



Internal ID15957026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:157091164..157187444hg38UCSC Ensembl
Innerchr4:158012316..158108596hg19UCSC Ensembl
Innerchr4:158231766..158328046hg18UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3896281
hg1996281
hg1896281
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv595804
Supporting Variants
Samples
Known GenesGLRB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1009756
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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