A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945800



Internal ID18245964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16849164..16955509hg38UCSC Ensembl
Innerchr1:17175659..17282004hg19UCSC Ensembl
Innerchr1:17047977..17154591hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38106346
hg19106346
hg18106615
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1754719, nssv1754723, nssv1754718, nssv1754721, nssv1754715, nssv1754716, nssv1754722, nssv1754717, nssv1755785, nssv1755786
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCROCC, MIR3675
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945800
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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