A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156709



Internal ID22087110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:108765008..108864876hg38UCSC Ensembl
Outerchr7:108762968..108865180hg38UCSC Ensembl
Innerchr7:108405452..108505320hg19UCSC Ensembl
Outerchr7:108403412..108505624hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38102213
hg19102213
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4022213
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156709
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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