A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156591



Internal ID22086992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:143548730..143551463hg38UCSC Ensembl
Outerchr6:143546656..143553010hg38UCSC Ensembl
Innerchr6:143869867..143872600hg19UCSC Ensembl
Outerchr6:143867793..143874147hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg386355
hg196355
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4022695, nssv4022694, nssv4022687, nssv4022690, nssv4022689, nssv4022693, nssv4022686, nssv4022692, nssv4022691, nssv4022688
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156591
Frequency
Sample Size131
Observed Gain3
Observed Loss7
Observed Complex0
Frequencyn/a


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