A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156234



Internal ID22086739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:139312369..139317206hg38UCSC Ensembl
Outerchr4:139311392..139318541hg38UCSC Ensembl
Innerchr4:140233523..140238360hg19UCSC Ensembl
Outerchr4:140232546..140239695hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg387150
hg197150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4015655, nssv4015659, nssv4015658, nssv4015657, nssv4015656
Samples
Known GenesNAA15
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156234
Frequency
Sample Size131
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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