A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1153641



Internal ID19199484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:104941910..104941961hg38UCSC Ensembl
Outerchr7:104582357..104582408hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4002295
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1153641
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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