A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4022156



Internal ID22083787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:85282038..85483231hg38UCSC Ensembl
Outerchr7:85277480..85484537hg38UCSC Ensembl
Innerchr7:84911354..85112547hg19UCSC Ensembl
Outerchr7:84906796..85113853hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38207058
hg19207058
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156693
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4022156
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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