A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972449



Internal ID18607665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:122749856..122750954hg38UCSC Ensembl
Innerchr9:125512135..125513233hg19UCSC Ensembl
Innerchr9:124551956..124553054hg18UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg381099
hg191099
hg181099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2566541, nssv2566543, nssv2566548, nssv2566546, nssv2566539, nssv2566544, nssv2566542, nssv2566545, nssv2566547, nssv2566540
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesOR1L6
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972449
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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