A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981529



Internal ID18270040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:74950172..74969837hg38UCSC Ensembl
Innerchr7:74365051..74383987hg19UCSC Ensembl
Innerchr7:74002987..74021923hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3819666
hg1918937
hg1818937
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2719414, nssv2719406, nssv2463216, nssv2719409, nssv2463222, nssv2463221, nssv2719410, nssv2463218, nssv2719407, nssv2463217, nssv2719413, nssv2719405, nssv2463223, nssv2719412, nssv2463215, nssv2463220, nssv2463214, nssv2719411, nssv2719408, nssv2463219
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)nsv981529
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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