A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966334



Internal ID18601564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:164189345..164190568hg38UCSC Ensembl
Innerchr4:165110497..165111720hg19UCSC Ensembl
Innerchr4:165329947..165331170hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg381224
hg191224
hg181224
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2340594, nssv2340592, nssv2340593, nssv2340599, nssv2340598, nssv2340595, nssv2340597, nssv2340601, nssv2340600, nssv2340596
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesMARCH1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv966334
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