A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981571



Internal ID18616768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:116968895..116977025hg38UCSC Ensembl
Innerchr7:116608949..116617079hg19UCSC Ensembl
Innerchr7:116396185..116404315hg18UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg388131
hg198131
hg188131
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2475756, nssv2475752, nssv2475753, nssv2475759, nssv2475758, nssv2475751, nssv2475754, nssv2475755, nssv2475757, nssv2475750
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesST7
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981571
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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