A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765057



Internal ID19307647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:150821712..150822213hg38UCSC Ensembl
chr3:150539499..150540000hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1073687
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765057
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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