A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156693



Internal ID22087094
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 Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4022156
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156693
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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