A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3767379



Internal ID18958803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:52533383..52534084hg38UCSC Ensembl
chr3:52567399..52568100hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg38702
hg19702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1072693
Supporting Variants
SamplesKWP1
Known GenesNT5DC2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3767379
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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