A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982197



Internal ID18617392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:15579329..15590305hg38UCSC Ensembl
Innerchr9:15579327..15590303hg19UCSC Ensembl
Innerchr9:15569327..15580303hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3810977
hg1910977
hg1810977
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2523009, nssv2523018, nssv2523014, nssv2523013, nssv2523015, nssv2523016, nssv2523017, nssv2523012, nssv2523010, nssv2523011
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCCDC171
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982197
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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