A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972417



Internal ID18607633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:92003912..92006994hg38UCSC Ensembl
Innerchr9:94766194..94769276hg19UCSC Ensembl
Innerchr9:93806015..93809097hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg383083
hg193083
hg183083
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2557158, nssv2557152, nssv2557153, nssv2557150, nssv2557151, nssv2557156, nssv2557157, nssv2557159, nssv2557155, nssv2557154
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)nsv972417
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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