A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968711



Internal ID18603939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:81990381..81993223hg38UCSC Ensembl
Innerchr9:84605296..84608138hg19UCSC Ensembl
Innerchr9:83795116..83797958hg18UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg382843
hg192843
hg182843
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2554225, nssv2554220, nssv2554227, nssv2554219, nssv2554226, nssv2554224, nssv2554223, nssv2554222, nssv2554218, nssv2554221
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesSPATA31D1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv968711
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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