A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1152516



Internal ID19200832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:108043570..108043693hg38UCSC Ensembl
Outerchr7:107684015..107684138hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3999698
SamplesKWB1
Known GenesLAMB4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1152516
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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