A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997667



Internal ID19157204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:121413177..121495660hg38UCSC Ensembl
Innerchr4:122334332..122416815hg19UCSC Ensembl
Innerchr4:122553782..122636265hg18UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3882484
hg1982484
hg1882484
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5379n100
Supporting Variantsnssv3639393
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997667
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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