A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv946231



Internal ID18593081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:149656308..149673215hg38UCSC Ensembl
Innerchr1:144452750..144472082hg19UCSC Ensembl
Innerchr1:143164107..143183439hg18UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg3816908
hg1919333
hg1819333
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1787469, nssv1787466, nssv1787460, nssv1787461, nssv1787463, nssv1787464, nssv1787465, nssv1787468, nssv1787467, nssv1787462
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLOC100288142
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv946231
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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