A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv946173



Internal ID18593023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:119085034..119086403hg38UCSC Ensembl
Innerchr1:119627657..119629026hg19UCSC Ensembl
Innerchr1:119429180..119430549hg18UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg381370
hg191370
hg181370
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1784218, nssv1784215, nssv1784217, nssv1784211, nssv1784216, nssv1784212, nssv1784214, nssv1784210, nssv1784209, nssv1784213
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)nsv946173
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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