A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969392



Internal ID18604619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:37084818..37093020hg38UCSC Ensembl
Innerchr6:37052594..37060796hg19UCSC Ensembl
Innerchr6:37160572..37168774hg18UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg388203
hg198203
hg188203
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2407609, nssv2407613, nssv2407612, nssv2407614, nssv2407610, nssv2407611, nssv2407608, nssv2407605, nssv2407607, nssv2407606
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
lineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv969392
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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