A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv961565



Internal ID18596811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:220048910..220049410hg38UCSC Ensembl
Innerchr2:220913631..220914131hg19UCSC Ensembl
Innerchr2:220621875..220622375hg18UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2219882, nssv2219876, nssv2219880, nssv2220676, nssv2219881, nssv2219879, nssv2219878, nssv2220677, nssv2219877, nssv2219883
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)nsv961565
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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