A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960449



Internal ID18595700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:26982040..27007049hg38UCSC Ensembl
Innerchr17:25309066..25334075hg19UCSC Ensembl
Innerchr17:22333193..22358202hg18UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg3825010
hg1925010
hg1825010
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2086805, nssv2086807, nssv2086803, nssv2086802, nssv2086806, nssv2086808, nssv2086804, nssv2086801, nssv2086810, nssv2086809
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv960449
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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