A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966768



Internal ID18601998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:27023979..27027154hg38UCSC Ensembl
Innerchr7:27063598..27066773hg19UCSC Ensembl
Innerchr7:27030123..27033298hg18UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg383176
hg193176
hg183176
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2439610, nssv2439607, nssv2439603, nssv2439608, nssv2439609, nssv2439612, nssv2439611, nssv2439606, nssv2439604, nssv2439605
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)nsv966768
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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