A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966306



Internal ID18601536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:108666231..108668878hg38UCSC Ensembl
Innerchr4:109587387..109590034hg19UCSC Ensembl
Innerchr4:109806836..109809483hg18UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg382648
hg192648
hg182648
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2330741, nssv2330735, nssv2330733, nssv2330742, nssv2330737, nssv2330734, nssv2330740, nssv2330739, nssv2330738, nssv2330736
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesOSTC
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv966306
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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