A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982414



Internal ID18617609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:65222275..65223124hg38UCSC Ensembl
Innerchr9:42779449..42780325hg19UCSC Ensembl
Innerchr9:42769445..42770321hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38850
hg19877
hg18877
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2730880, nssv2730874, nssv2730877, nssv2730875, nssv2730872, nssv2730879, nssv2730878, nssv2730873, nssv2730876, nssv2730871
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982414
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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