A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969341



Internal ID18604568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:62000..102888hg38UCSC Ensembl
Innerchr6:62000..102888hg19UCSC Ensembl
Innerchr6:7000..47888hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3840889
hg1940889
hg1840889
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2390956, nssv2390948, nssv2390950, nssv2390951, nssv2390953, nssv2390952, nssv2390955, nssv2390957, nssv2390949, nssv2390954
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)nsv969341
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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