A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968736



Internal ID18603964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:96407251..96409605hg38UCSC Ensembl
Innerchr9:99169533..99171887hg19UCSC Ensembl
Innerchr9:98209354..98211708hg18UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg382355
hg192355
hg182355
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2560176, nssv2560179, nssv2560178, nssv2560173, nssv2560174, nssv2560180, nssv2560175, nssv2560171, nssv2560172, nssv2560177
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesZNF367
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv968736
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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