A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945977



Internal ID18246141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:63841486..63844662hg38UCSC Ensembl
Innerchr1:64307157..64310333hg19UCSC Ensembl
Innerchr1:64079745..64082921hg18UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg383177
hg193177
hg183177
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1770508, nssv1770512, nssv1770509, nssv1770510, nssv1770507, nssv1770515, nssv1770513, nssv1770514, nssv1770511, nssv1770506
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesROR1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945977
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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