A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4022222



Internal ID22083853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:113507462..113513537hg38UCSC Ensembl
Outerchr7:113505196..113524413hg38UCSC Ensembl
Innerchr7:113147517..113153592hg19UCSC Ensembl
Outerchr7:113145251..113164468hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3819218
hg1919218
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156716
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4022222
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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