A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965723



Internal ID18600953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:46850402..46860523hg38UCSC Ensembl
Innerchr6:46818139..46828260hg19UCSC Ensembl
Innerchr6:46926098..46936219hg18UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3810122
hg1910122
hg1810122
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2406825, nssv2406819, nssv2406817, nssv2406820, nssv2406823, nssv2406816, nssv2406818, nssv2406821, nssv2406824, nssv2406822
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesGPR116
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965723
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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