A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156202



Internal ID22086707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:96399079..96401252hg38UCSC Ensembl
Outerchr4:96395896..96405817hg38UCSC Ensembl
Innerchr4:97320230..97322403hg19UCSC Ensembl
Outerchr4:97317047..97326968hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg389922
hg199922
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4014728, nssv4014726, nssv4014729, nssv4014727
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156202
Frequency
Sample Size131
Observed Gain1
Observed Loss3
Observed Complex0
Frequencyn/a


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