A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv961960



Internal ID18597206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:91441118..91443785hg38UCSC Ensembl
Innerchr2:91633662..91636327hg19UCSC Ensembl
Innerchr2:90997389..91000054hg18UCSC Ensembl
Cytoband2p11.1
Allele length
AssemblyAllele length
hg382668
hg192666
hg182666
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2664421, nssv2664383, nssv2664387, nssv2664418, nssv2664384, nssv2664392, nssv2664386, nssv2664420, nssv2664390, nssv2664385, nssv2664389, nssv2664422, nssv2664423, nssv2664416, nssv2664417, nssv2664424, nssv2664388, nssv2664391, nssv2664425, nssv2664419
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv961960
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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