A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969424



Internal ID18604651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:85426979..85427912hg38UCSC Ensembl
Innerchr6:86136697..86137630hg19UCSC Ensembl
Innerchr6:86193416..86194349hg18UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg38934
hg19934
hg18934
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2415611, nssv2415612, nssv2415614, nssv2415616, nssv2415619, nssv2415618, nssv2415615, nssv2415613, nssv2415610, nssv2415617
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)nsv969424
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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