A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945963



Internal ID18592813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:55787231..55793098hg38UCSC Ensembl
Innerchr1:56252904..56258771hg19UCSC Ensembl
Innerchr1:56025492..56031359hg18UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg385868
hg195868
hg185868
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1768920, nssv1768927, nssv1768918, nssv1768922, nssv1768923, nssv1768925, nssv1768921, nssv1768924, nssv1768919, nssv1768926
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)nsv945963
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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