A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156124



Internal ID22086629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:22047010..22069078hg38UCSC Ensembl
Outerchr4:22043756..22072923hg38UCSC Ensembl
Innerchr4:22048633..22070701hg19UCSC Ensembl
Outerchr4:22045379..22074546hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3829168
hg1929168
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4014116
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156124
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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