A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981205



Internal ID18616404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:166335108..166337668hg38UCSC Ensembl
Innerchr6:166748596..166751156hg19UCSC Ensembl
Innerchr6:166668586..166671146hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg382561
hg192561
hg182561
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2431136, nssv2431139, nssv2431141, nssv2431143, nssv2431135, nssv2431140, nssv2431142, nssv2431137, nssv2431138, nssv2431134
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesSFT2D1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981205
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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