A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2758382



Internal ID17733075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:95978514..95995838hg38UCSC Ensembl
Innerchr3:95697358..95714682hg19UCSC Ensembl
Innerchr3:97180048..97197372hg18UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3817325
hg1917325
hg1817325
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv967243
Supporting Variants
SamplesHGDP00456
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2758382
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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