A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977956



Internal ID18266475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:30218194..30257796hg38UCSC Ensembl
Innerchr16:30229515..30269117hg19UCSC Ensembl
Innerchr16:30137016..30176618hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3839603
hg1939603
hg1839603
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2056517, nssv2056365, nssv2056369, nssv2056514, nssv2056516, nssv2056366, nssv2056515, nssv2056364, nssv2056367, nssv2056368
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesLOC613037
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977956
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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