A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv946174



Internal ID18593024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:119116161..119127878hg38UCSC Ensembl
Innerchr1:119658784..119670501hg19UCSC Ensembl
Innerchr1:119460307..119472024hg18UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg3811718
hg1911718
hg1811718
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1784310, nssv1784311, nssv1784307, nssv1784309, nssv1784306, nssv1784308, nssv1784313, nssv1784312, nssv1784314, nssv1784315
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesWARS2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv946174
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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