A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972290



Internal ID18607506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:137896..182124hg38UCSC Ensembl
Innerchr9:137896..182124hg19UCSC Ensembl
Innerchr9:127896..172124hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3844229
hg1944229
hg1844229
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2520252, nssv2520253, nssv2520251, nssv2520248, nssv2520249, nssv2520254, nssv2520250, nssv2520255, nssv2520256, nssv2520257
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCBWD1
MethodSequencing
Analysislineage specific fixed duplications
lineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972290
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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