A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154656



Internal ID22085161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:112352317..112357081hg38UCSC Ensembl
Outerchr10:112351590..112358659hg38UCSC Ensembl
Innerchr10:114112075..114116839hg19UCSC Ensembl
Outerchr10:114111348..114118417hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg387070
hg197070
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4004501, nssv4004489, nssv4004526, nssv4004472, nssv4004491, nssv4004475, nssv4004515, nssv4004476, nssv4004474, nssv4004516, nssv4004505, nssv4004512, nssv4004503, nssv4004495, nssv4004494, nssv4004484, nssv4004482, nssv4004506, nssv4004514, nssv4004518, nssv4004523, nssv4004499, nssv4004520, nssv4004478, nssv4004483, nssv4004513, nssv4004477, nssv4004502, nssv4004492, nssv4004504, nssv4004511, nssv4004507, nssv4004486, nssv4004517, nssv4004510, nssv4004480, nssv4004488, nssv4004479, nssv4004493, nssv4004524, nssv4004470, nssv4004469, nssv4004497, nssv4004485, nssv4004525, nssv4004490, nssv4004522, nssv4004521, nssv4004473, nssv4004471, nssv4004498, nssv4004496, nssv4004487, nssv4004481, nssv4004509, nssv4004500, nssv4004519, nssv4004468, nssv4004508
Samples
Known GenesGUCY2GP
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154656
Frequency
Sample Size131
Observed Gain59
Observed Loss0
Observed Complex0
Frequencyn/a


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