A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156596



Internal ID22086997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:154642532..154650798hg38UCSC Ensembl
Outerchr6:154639748..154654106hg38UCSC Ensembl
Innerchr6:154963666..154971932hg19UCSC Ensembl
Outerchr6:154960882..154975240hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3814359
hg1914359
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4022701, nssv4022703, nssv4022702
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156596
Frequency
Sample Size131
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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