A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1152842



Internal ID19196171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:104974761..104975088hg38UCSC Ensembl
Outerchr7:104615208..104615535hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3997877
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1152842
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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