A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966863



Internal ID18602092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:98453056..98455652hg38UCSC Ensembl
Innerchr7:98082368..98084964hg19UCSC Ensembl
Innerchr7:97920304..97922900hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg382597
hg192597
hg182597
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2470534, nssv2470535, nssv2470536, nssv2470533, nssv2470540, nssv2470538, nssv2470537, nssv2470541, nssv2470532, nssv2470539
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
lineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv966863
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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