A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947850



Internal ID18594697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:37601553..37603627hg38UCSC Ensembl
Innerchr10:37890481..37892555hg19UCSC Ensembl
Innerchr10:37930487..37932561hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg382075
hg192075
hg182075
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1840183, nssv1840188, nssv1840191, nssv1840185, nssv1840192, nssv1840184, nssv1840189, nssv1840186, nssv1840190, nssv1840187
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesMTRNR2L7
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947850
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