A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945841



Internal ID18246005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:26452485..26456064hg38UCSC Ensembl
Innerchr1:26778976..26782555hg19UCSC Ensembl
Innerchr1:26651563..26655142hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg383580
hg193580
hg183580
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1765542, nssv1765541, nssv1765540, nssv1765534, nssv1765537, nssv1765539, nssv1765538, nssv1765535, nssv1765533, nssv1765536
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesDHDDS
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945841
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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