A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966335



Internal ID18254879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:164196402..164197687hg38UCSC Ensembl
Innerchr4:165117554..165118839hg19UCSC Ensembl
Innerchr4:165337004..165338289hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg381286
hg191286
hg181286
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2339126, nssv2339123, nssv2339121, nssv2339117, nssv2339118, nssv2339119, nssv2339122, nssv2339124, nssv2339120, nssv2339125
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesANP32C, MARCH1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv966335
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer