A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv971339



Internal ID18606559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:96068715..96079568hg38UCSC Ensembl
Innerchr8:97080943..97091796hg19UCSC Ensembl
Innerchr8:97150119..97160972hg18UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3810854
hg1910854
hg1810854
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2514325, nssv2514327, nssv2514322, nssv2514321, nssv2514320, nssv2514318, nssv2514323, nssv2514326, nssv2514324, nssv2514319
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)nsv971339
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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