A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966872



Internal ID18602101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:103151304..103158058hg38UCSC Ensembl
Innerchr7:102791751..102798505hg19UCSC Ensembl
Innerchr7:102578987..102585741hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg386755
hg196755
hg186755
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2474519, nssv2474522, nssv2474526, nssv2474524, nssv2474527, nssv2474520, nssv2474528, nssv2474521, nssv2474525, nssv2474523
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)nsv966872
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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