A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3764448



Internal ID18961487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:21241638..21242339hg38UCSC Ensembl
chr18:18821599..18822300hg19UCSC Ensembl
Cytoband18q11.1
Allele length
AssemblyAllele length
hg38702
hg19702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1071443
Supporting Variants
SamplesKWP1
Known GenesGREB1L
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3764448
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