A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972800



Internal ID18608016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112173325..112175563hg38UCSC Ensembl
Innerchr9:114935605..114937843hg19UCSC Ensembl
Innerchr9:113975426..113977664hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg382239
hg192239
hg182239
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2565531, nssv2565528, nssv2565522, nssv2565524, nssv2565526, nssv2565527, nssv2565530, nssv2565525, nssv2565529, nssv2565523
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesMIR3134, SUSD1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972800
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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