A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972306



Internal ID18607522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33486355..33510885hg38UCSC Ensembl
Innerchr9:33486353..33510883hg19UCSC Ensembl
Innerchr9:33476353..33500883hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3824531
hg1924531
hg1824531
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2526538, nssv2526541, nssv2526539, nssv2526540, nssv2526543, nssv2526542, nssv2526546, nssv2526544, nssv2526547, nssv2526545
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesSUGT1P1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972306
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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