A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945939



Internal ID18592789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:51157653..51158246hg38UCSC Ensembl
Innerchr1:51623325..51623918hg19UCSC Ensembl
Innerchr1:51395913..51396506hg18UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38594
hg19594
hg18594
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1767173, nssv1767170, nssv1767174, nssv1767175, nssv1767171, nssv1767178, nssv1767172, nssv1767176, nssv1767179, nssv1767177
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)nsv945939
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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