A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982204



Internal ID18617399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:26878628..26880451hg38UCSC Ensembl
Innerchr9:26878626..26880449hg19UCSC Ensembl
Innerchr9:26868626..26870449hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg381824
hg191824
hg181824
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2524884, nssv2524886, nssv2524880, nssv2524881, nssv2524885, nssv2524883, nssv2524889, nssv2524887, nssv2524882, nssv2524888
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCAAP1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982204
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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