A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972661



Internal ID18261191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33381481..33395414hg38UCSC Ensembl
Innerchr9:33381479..33395412hg19UCSC Ensembl
Innerchr9:33371479..33385412hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3813934
hg1913934
hg1813934
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2526338, nssv2526334, nssv2526333, nssv2526337, nssv2526335, nssv2526332, nssv2526336, nssv2526340, nssv2526339, nssv2526341
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesAQP7
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972661
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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