A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945884



Internal ID18592734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:37840834..37844110hg38UCSC Ensembl
Innerchr1:38306506..38309782hg19UCSC Ensembl
Innerchr1:38079093..38082369hg18UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg383277
hg193277
hg183277
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1760141, nssv1760140, nssv1760143, nssv1760142, nssv1760149, nssv1760145, nssv1760147, nssv1760148, nssv1760144, nssv1760146
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesMTF1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945884
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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