A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972463



Internal ID18607679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135519952..135526968hg38UCSC Ensembl
Innerchr9:138411798..138418814hg19UCSC Ensembl
Innerchr9:137551619..137558635hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg387017
hg197017
hg187017
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2570397, nssv2570401, nssv2570398, nssv2570399, nssv2570400, nssv2570396, nssv2570405, nssv2570403, nssv2570402, nssv2570404
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLCN1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972463
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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