A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4001142



Internal ID19188354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:68395329..68395443hg38UCSC Ensembl
Outerchr7:67860316..67860430hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1153225
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4001142
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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