A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945844



Internal ID18592694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:26975557..26986879hg38UCSC Ensembl
Innerchr1:27302048..27313370hg19UCSC Ensembl
Innerchr1:27174635..27185957hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3811323
hg1911323
hg1811323
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1765335, nssv1765327, nssv1765331, nssv1765333, nssv1765336, nssv1765328, nssv1765332, nssv1765330, nssv1765329, nssv1765334
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945844
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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