A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964032



Internal ID18252584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:9783203..9800987hg38UCSC Ensembl
Innerchr4:9784827..9802611hg19UCSC Ensembl
Innerchr4:9393925..9411709hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3817785
hg1917785
hg1817785
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2313198, nssv2313199, nssv2313201, nssv2313200, nssv2313204, nssv2313205, nssv2313197, nssv2313203, nssv2313206, nssv2313202
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesDRD5
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv964032
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