A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968729



Internal ID18603957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:91168017..91169951hg38UCSC Ensembl
Innerchr9:93930299..93932233hg19UCSC Ensembl
Innerchr9:92970120..92972054hg18UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg381935
hg191935
hg181935
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2557054, nssv2557055, nssv2557059, nssv2557061, nssv2557060, nssv2557056, nssv2557057, nssv2557062, nssv2557058, nssv2557053
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)nsv968729
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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