A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4021052



Internal ID22082683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:10752523..10766481hg38UCSC Ensembl
Outerchr7:10740864..10768058hg38UCSC Ensembl
Innerchr7:10792150..10806108hg19UCSC Ensembl
Outerchr7:10780491..10807685hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3827195
hg1927195
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156644
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4021052
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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