A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv979906



Internal ID18615107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:180820747..180826493hg38UCSC Ensembl
Innerchr3:180538535..180544281hg19UCSC Ensembl
Innerchr3:182021229..182026975hg18UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg385747
hg195747
hg185747
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2305697, nssv2305693, nssv2305695, nssv2305692, nssv2305698, nssv2305691, nssv2305696, nssv2305699, nssv2305694, nssv2305690
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv979906
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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