A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964808



Internal ID18600044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:181351190..181371476hg38UCSC Ensembl
Innerchr5:180778191..180798477hg19UCSC Ensembl
Innerchr5:180710797..180731083hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3820287
hg1920287
hg1820287
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2391697, nssv2391694, nssv2391696, nssv2391688, nssv2391693, nssv2391689, nssv2391690, nssv2391695, nssv2391691, nssv2391692
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesOR4F16, OR4F29, OR4F3
MethodSequencing
Analysislineage specific fixed deletions
lineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv964808
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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