A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970150



Internal ID18605374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:85287618..85289033hg38UCSC Ensembl
Innerchr6:85997336..85998751hg19UCSC Ensembl
Innerchr6:86054055..86055470hg18UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg381416
hg191416
hg181416
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2415522, nssv2415516, nssv2415515, nssv2415513, nssv2415519, nssv2415514, nssv2415517, nssv2415518, nssv2415521, nssv2415520
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)nsv970150
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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