A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966881



Internal ID18602110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:122229465..122244613hg38UCSC Ensembl
Innerchr7:121869519..121884667hg19UCSC Ensembl
Innerchr7:121656755..121671903hg18UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg3815149
hg1915149
hg1815149
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2475908, nssv2475913, nssv2475911, nssv2475909, nssv2475916, nssv2475912, nssv2475917, nssv2475910, nssv2475914, nssv2475915
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)nsv966881
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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