A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv971950



Internal ID18607166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:56576694..56577694hg38UCSC Ensembl
Innerchr11:56344170..56345170hg19UCSC Ensembl
Innerchr11:56100746..56101746hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg381001
hg191001
hg181001
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1888032, nssv1888026, nssv1888030, nssv1888034, nssv1888031, nssv1888033, nssv1888025, nssv1888029, nssv1888027, nssv1888028
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesOR5M10
MethodSequencing
Analysislineage specific fixed deletions
lineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv971950
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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