A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3772399



Internal ID18964575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:8678369..8679270hg38UCSC Ensembl
chr2:8818499..8819400hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38902
hg19902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1072386
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3772399
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