A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv961035



Internal ID18596282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:14935357..14984975hg38UCSC Ensembl
Innerchr18:14935356..14984974hg19UCSC Ensembl
Innerchr18:14925356..14974974hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3849619
hg1949619
hg1849619
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2119561, nssv2119560, nssv2119563, nssv2119567, nssv2119564, nssv2119566, nssv2119565, nssv2119562, nssv2119569, nssv2119568
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLOC400644
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv961035
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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