A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv988547



Internal ID16282503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:2261514..2262338hg38UCSC Ensembl
Innerchr4:2263241..2264065hg19UCSC Ensembl
Innerchr4:2233039..2233863hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38825
hg19825
hg18825
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593391
Supporting Variants
Samples
Known GenesMXD4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv988547
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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