A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765780



Internal ID19313464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:90326537..90402511hg38UCSC Ensembl
chr2:90371499..90447500hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg3875975
hg1976002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1077874
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765780
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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