A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945269



Internal ID18245457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:207676101..207712783hg38UCSC Ensembl
Innerchr1:207849446..207886128hg19UCSC Ensembl
Innerchr1:205916069..205952751hg18UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3836683
hg1936683
hg1836683
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1815502, nssv1815503, nssv1815500, nssv1815505, nssv1815501, nssv1815509, nssv1815508, nssv1815506, nssv1815507, nssv1815504
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCR1L
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945269
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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