A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv971971



Internal ID18607187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3386452..3605250hg38UCSC Ensembl
Innerchr11:3407682..3626480hg19UCSC Ensembl
Innerchr11:3364258..3583056hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38218799
hg19218799
hg18218799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1872675, nssv1872677, nssv1872668, nssv1872672, nssv1872676, nssv1872669, nssv1872671, nssv1872670, nssv1872673, nssv1872674
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLOC650368, OR7E12P
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv971971
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer