A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981965



Internal ID18617161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:93847317..93854416hg38UCSC Ensembl
Innerchr8:94859545..94866644hg19UCSC Ensembl
Innerchr8:94928721..94935820hg18UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg387100
hg197100
hg187100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2513014, nssv2513008, nssv2513009, nssv2513011, nssv2513010, nssv2513013, nssv2513016, nssv2513015, nssv2513017, nssv2513012
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)nsv981965
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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