A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv973275



Internal ID18608490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42890322..42896180hg38UCSC Ensembl
Innerchr9:44074939..44080797hg19UCSC Ensembl
Innerchr9:44014935..44020793hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg385859
hg195859
hg185859
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2733641, nssv2733635, nssv2733707, nssv2733715, nssv2733714, nssv2733713, nssv2733712, nssv2733708, nssv2733639, nssv2733643, nssv2733637, nssv2733709, nssv2733710, nssv2733706, nssv2733638, nssv2733640, nssv2733642, nssv2733644, nssv2733636, nssv2733711
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)nsv973275
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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