A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982297



Internal ID18617492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:65830543..65846000hg38UCSC Ensembl
Innerchr9:70318730..70335502hg19UCSC Ensembl
Innerchr9:69558373..69575322hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3815458
hg1916773
hg1816950
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2752446, nssv2753019, nssv2756274, nssv2747759, nssv2755648, nssv2750226, nssv2751405, nssv2751704, nssv2754792, nssv2752008
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)nsv982297
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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