A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972799



Internal ID18608015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:111606619..111610015hg38UCSC Ensembl
Innerchr9:114368899..114372295hg19UCSC Ensembl
Innerchr9:113408720..113412116hg18UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg383397
hg193397
hg183397
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2565432, nssv2565425, nssv2565431, nssv2565433, nssv2565429, nssv2565426, nssv2565427, nssv2565428, nssv2565434, nssv2565430
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLRRC37A5P
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972799
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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