A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv971766



Internal ID18606983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:73694370..73698667hg38UCSC Ensembl
Innerchr10:75454128..75458425hg19UCSC Ensembl
Innerchr10:75124134..75128431hg18UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg384298
hg194298
hg184298
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2615951, nssv2615949, nssv2615952, nssv2615950, nssv2615947, nssv2615948, nssv2615945, nssv2615946, nssv2615953, nssv2615954
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesAGAP5
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv971766
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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