A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965410



Internal ID18600644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:175359852..175370396hg38UCSC Ensembl
Innerchr3:175077641..175088185hg19UCSC Ensembl
Innerchr3:176560335..176570879hg18UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3810545
hg1910545
hg1810545
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2758444, nssv2758070, nssv2760238
SamplesHGDP01284, HGDP00665, HGDP00998
Known GenesMIR4789, NAALADL2
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965410
Frequency
Sample Size10
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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