A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966780



Internal ID18602010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:38334742..38368274hg38UCSC Ensembl
Innerchr7:38374343..38407875hg19UCSC Ensembl
Innerchr7:38340868..38374400hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3833533
hg1933533
hg1833533
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2442993, nssv2442986, nssv2442992, nssv2442994, nssv2442985, nssv2442987, nssv2442990, nssv2442991, nssv2442988, nssv2442989
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesTRG-AS1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv966780
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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