A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982541



Internal ID18617736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:82433551..82438004hg38UCSC Ensembl
Innerchr9:85048466..85052919hg19UCSC Ensembl
Innerchr9:84238286..84242739hg18UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg384454
hg194454
hg184454
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2751888, nssv2751385, nssv2751727, nssv2755469, nssv2748354, nssv2749981, nssv2756429, nssv2753770, nssv2750582, nssv2747119
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)nsv982541
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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