A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2430449



Internal ID17786267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160698507..160700485hg38UCSC Ensembl
Innerchr6:161119539..161121517hg19UCSC Ensembl
Innerchr6:161039529..161041507hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg381979
hg191979
hg181979
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv970188
Supporting Variants
SamplesHGDP00665
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2430449
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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