A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982495



Internal ID18617690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:67903064..67905125hg38UCSC Ensembl
Innerchr9:67970510..67972571hg19UCSC Ensembl
Innerchr9:67560330..67562391hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg382062
hg192062
hg182062
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2742521, nssv2742520, nssv2741569, nssv2742517, nssv2741567, nssv2742522, nssv2741571, nssv2742518, nssv2741574, nssv2741575, nssv2741570, nssv2743318, nssv2741576, nssv2742523, nssv2741573, nssv2742519, nssv2741568, nssv2743317, nssv2743316, nssv2741572
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982495
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