A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765856



Internal ID18958607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:4008343..4008427hg38UCSC Ensembl
chr20:3988990..3989074hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1073040
Supporting Variants
SamplesKWP1
Known GenesRNF24
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765856
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