A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945831



Internal ID18245995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25260030..25293460hg38UCSC Ensembl
Innerchr1:25586521..25619951hg19UCSC Ensembl
Innerchr1:25459108..25492538hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3833431
hg1933431
hg1833431
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1766629, nssv1766627, nssv1766636, nssv1766631, nssv1766630, nssv1766633, nssv1766634, nssv1766635, nssv1766628, nssv1766632
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesRHD
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945831
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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