A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981105



Internal ID18616304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:12319450..12320191hg38UCSC Ensembl
Innerchr6:12319682..12320423hg19UCSC Ensembl
Innerchr6:12427668..12428409hg18UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg38742
hg19742
hg18742
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2393398, nssv2393396, nssv2393400, nssv2393395, nssv2393397, nssv2393393, nssv2393401, nssv2393394, nssv2393399, nssv2393392
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)nsv981105
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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