A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945753



Internal ID18592604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:5665755..5676552hg38UCSC Ensembl
Innerchr1:5725815..5736612hg19UCSC Ensembl
Innerchr1:5648402..5659199hg18UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg3810798
hg1910798
hg1810798
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1750342, nssv1750348, nssv1750346, nssv1750345, nssv1750343, nssv1750350, nssv1750349, nssv1750344, nssv1750341, nssv1750347
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
lineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945753
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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