A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150671



Internal ID19199205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:120977181..120977272hg38UCSC Ensembl
Outerchr6:121298327..121298418hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3996146
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150671
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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