A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981924



Internal ID18617120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:29294405..29315464hg38UCSC Ensembl
Innerchr8:29151922..29172981hg19UCSC Ensembl
Innerchr8:29207841..29228900hg18UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3821060
hg1921060
hg1821060
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2498075, nssv2498079, nssv2498082, nssv2498078, nssv2498077, nssv2498076, nssv2498081, nssv2498080, nssv2498073, nssv2498074
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981924
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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