A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968733



Internal ID18603961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:94315642..94337534hg38UCSC Ensembl
Innerchr9:97077924..97099816hg19UCSC Ensembl
Innerchr9:96117745..96139637hg18UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3821893
hg1921893
hg1821893
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2560434, nssv2560436, nssv2560439, nssv2560431, nssv2560435, nssv2560432, nssv2560430, nssv2560438, nssv2560433, nssv2560437
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLOC100132077, NUTM2F
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv968733
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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