A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967786



Internal ID18603014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:112564998..112566718hg38UCSC Ensembl
Innerchr4:113486154..113487874hg19UCSC Ensembl
Innerchr4:113705603..113707323hg18UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg381721
hg191721
hg181721
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2332659, nssv2332652, nssv2332661, nssv2332655, nssv2332658, nssv2332656, nssv2332657, nssv2332660, nssv2332653, nssv2332654
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesC4orf21
MethodSequencing
Analysislineage specific fixed duplications
lineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv967786
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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