A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945867



Internal ID18592717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:31486145..31488336hg38UCSC Ensembl
Innerchr1:31958992..31961183hg19UCSC Ensembl
Innerchr1:31731579..31733770hg18UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg382192
hg192192
hg182192
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1757589, nssv1757581, nssv1757584, nssv1757588, nssv1757590, nssv1757585, nssv1757582, nssv1757586, nssv1757583, nssv1757587
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)nsv945867
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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