A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1147877



Internal ID19195565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:135100955..135101010hg38UCSC Ensembl
Outerchr6:135422093..135422148hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3996664
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1147877
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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