A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972699



Internal ID18607915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:60971677..60999027hg38UCSC Ensembl
Innerchr9:41557949..41585299hg19UCSC Ensembl
Innerchr9:41547949..41575299hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3827351
hg1927351
hg1827351
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2534342, nssv2534340, nssv2534337, nssv2534343, nssv2534341, nssv2534336, nssv2534345, nssv2534338, nssv2534339, nssv2534344
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)nsv972699
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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