A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970112



Internal ID18605336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:41663156..41670735hg38UCSC Ensembl
Innerchr6:41630894..41638473hg19UCSC Ensembl
Innerchr6:41738872..41746451hg18UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg387580
hg197580
hg187580
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2408707, nssv2408713, nssv2408712, nssv2408706, nssv2408708, nssv2408714, nssv2408710, nssv2408709, nssv2408705, nssv2408711
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)nsv970112
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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