A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970163



Internal ID18605387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:126642848..126646093hg38UCSC Ensembl
Innerchr6:126963994..126967239hg19UCSC Ensembl
Innerchr6:127005687..127008932hg18UCSC Ensembl
Cytoband6q22.32
Allele length
AssemblyAllele length
hg383246
hg193246
hg183246
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2422716, nssv2422714, nssv2422717, nssv2422715, nssv2422708, nssv2422709, nssv2422713, nssv2422711, nssv2422712, nssv2422710
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)nsv970163
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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