A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981101



Internal ID18616300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:5787409..5788647hg38UCSC Ensembl
Innerchr6:5787642..5788880hg19UCSC Ensembl
Innerchr6:5732641..5733879hg18UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg381239
hg191239
hg181239
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2393095, nssv2393096, nssv2393093, nssv2393100, nssv2393099, nssv2393091, nssv2393092, nssv2393094, nssv2393097, nssv2393098
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)nsv981101
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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