A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972409



Internal ID18607625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:85745331..85806220hg38UCSC Ensembl
Innerchr9:88360246..88421135hg19UCSC Ensembl
Innerchr9:87550066..87610955hg18UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3860890
hg1960890
hg1860890
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2554060, nssv2554059, nssv2554054, nssv2554056, nssv2554057, nssv2554058, nssv2554062, nssv2554063, nssv2554055, nssv2554061
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLOC389765
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972409
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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