A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156650



Internal ID22087051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:19898785..19900500hg38UCSC Ensembl
Outerchr7:19895444..19909147hg38UCSC Ensembl
Innerchr7:19938408..19940123hg19UCSC Ensembl
Outerchr7:19935067..19948770hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3813704
hg1913704
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4021060
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156650
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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