A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982392



Internal ID18617587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39821175..39825473hg38UCSC Ensembl
Innerchr9:41966193..41970491hg19UCSC Ensembl
Innerchr9:41956193..41960491hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg384299
hg194299
hg184299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2727450, nssv2727444, nssv2727449, nssv2727443, nssv2727452, nssv2727451, nssv2727445, nssv2727446, nssv2727447, nssv2727448
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesKGFLP2
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982392
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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