A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970168



Internal ID18605392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:132997395..132997895hg38UCSC Ensembl
Innerchr6:133318534..133319034hg19UCSC Ensembl
Innerchr6:133360227..133360727hg18UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2424275, nssv2424279, nssv2424283, nssv2424278, nssv2424280, nssv2424276, nssv2424281, nssv2424277, nssv2424284, nssv2424282
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
lineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970168
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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