A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4022183



Internal ID22083814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:91402027..91411412hg38UCSC Ensembl
Outerchr7:91400153..91417678hg38UCSC Ensembl
Innerchr7:91031342..91040727hg19UCSC Ensembl
Outerchr7:91029468..91046993hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3817526
hg1917526
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156699
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4022183
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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