A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv961560



Internal ID18250120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:218134916..218135916hg38UCSC Ensembl
Innerchr2:218999639..219000639hg19UCSC Ensembl
Innerchr2:218707884..218708884hg18UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg381001
hg191001
hg181001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2221798, nssv2221807, nssv2221804, nssv2221799, nssv2221803, nssv2221802, nssv2221806, nssv2221805, nssv2221800, nssv2221801
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCXCR2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv961560
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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