A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972781



Internal ID18607997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:92876976..92909462hg38UCSC Ensembl
Innerchr9:95639258..95671744hg19UCSC Ensembl
Innerchr9:94679079..94711565hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3832487
hg1932487
hg1832487
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2559991, nssv2559997, nssv2559990, nssv2559992, nssv2559996, nssv2559994, nssv2559988, nssv2559993, nssv2559989, nssv2559995
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesZNF484
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972781
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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