A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981203



Internal ID18616402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160598984..160662125hg38UCSC Ensembl
Innerchr6:161020016..161083157hg19UCSC Ensembl
Innerchr6:160940006..161003147hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3863142
hg1963142
hg1863142
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2429457, nssv2429464, nssv2429455, nssv2429458, nssv2429459, nssv2429456, nssv2429461, nssv2429462, nssv2429463, nssv2429460
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLPA
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981203
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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