A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970069



Internal ID18605293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:144819..155708hg38UCSC Ensembl
Innerchr6:144819..155708hg19UCSC Ensembl
Innerchr6:89819..100708hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3810890
hg1910890
hg1810890
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2391159, nssv2391163, nssv2391157, nssv2391162, nssv2391156, nssv2391158, nssv2391160, nssv2391165, nssv2391164, nssv2391161
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)nsv970069
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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