A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969646



Internal ID18604873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:63023326..63024175hg38UCSC Ensembl
Innerchr9:66928298..66929147hg19UCSC Ensembl
Innerchr9:66668118..66668967hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38850
hg19850
hg18850
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2738119, nssv2738112, nssv2738113, nssv2738118, nssv2738116, nssv2738110, nssv2738114, nssv2738115, nssv2738117, nssv2738111
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)nsv969646
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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