A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv971664



Internal ID18606881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:73215988..73216587hg38UCSC Ensembl
Innerchr8:74128223..74128822hg19UCSC Ensembl
Innerchr8:74290777..74291376hg18UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg38600
hg19600
hg18600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2508790, nssv2508787, nssv2508788, nssv2508784, nssv2508783, nssv2508791, nssv2508785, nssv2508786, nssv2508792, nssv2508789
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)nsv971664
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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