A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156721



Internal ID22087122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:120996879..121016574hg38UCSC Ensembl
Outerchr7:120996742..121020676hg38UCSC Ensembl
Innerchr7:120636933..120656628hg19UCSC Ensembl
Outerchr7:120636796..120660730hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg3823935
hg1923935
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4022227
Samples
Known GenesCPED1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156721
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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