A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945265



Internal ID18592116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:447598..467031hg38UCSC Ensembl
Innerchr1:352306..371739hg19UCSC Ensembl
Innerchr1:342169..361602hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3819434
hg1919434
hg1819434
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1756441, nssv1756439, nssv1756444, nssv1756440, nssv1756447, nssv1756443, nssv1756438, nssv1756445, nssv1756442, nssv1756446
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)nsv945265
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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